# FewerJobs export - 100 curated jobs Generated: 2026-06-18T21:49:19.408Z Source: https://fewerjobs.com ## Filters applied - **q**: Standard Biotools Inc - **quality_floor**: default - **match_401k_strict**: true - **parental_strict**: true - **non_birth_strict**: true - **pto_strict**: true - **include_older**: false - **verified_benefits_only**: true - **apply_url_verified**: false - **page**: 1 - **per_page**: 100 - **sort**: relevance ## Jobs ### Senior Scientific Director, International Medical Affairs – Gastroenterology: Cross-IBD / Standard of Care Lead - AbbVie Inc. - Location: Mettawa, IL, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013173636-senior-scientific-director-international-medical-affairs-gastroenterology-cross-ibd-standard-of-care-lead- - Excerpt: Senior Scientific Director, International Medical Affairs – Gastroenterology: Cross-IBD / Standard of Care Lead Mettawa, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The Medical Affairs organization provides patients, healthcare providers, and payers everywhere with the practical and clinically relevant information and solutions they need to use AbbVie products safely and effectively, throughout the product lifecycle and the patient's journey. The Senior Scientific Director, International Medical Affairs provides specialist medical and scientific input into core strategic and operational medical affairs activities for the International Gastroenterology portfolio such as: health-care professional and provider interactions; generation of clinical and scientific data (enhancing therapeutic benefit and value); educational initiatives, scientific communications, value propositioning, and safeguarding patient safety (risk minimization activities and safety surveillance activities). As the Cross-IBD and Standard of Care Lead, you will work closely with marketing and commercial teams to provide strategic medical input into strategies to elevate standard of care in IBD. Other key deliverables include leading evidence generation plans and tactics, driving scientific communication initiatives (both internal and external medical education, data, ### Naval Standard Missile Systems (NSMS) - Principal Program Controls Specialist - Raytheon Technologies - Location: US-AZ-TUCSON-802 ~ 1151 E Hermans Rd ~ BLDG 802 (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Parental leave: 4 weeks (not source-backed) - Non-birth-parent leave: 4 weeks (not source-backed) - Apply: https://globalhr.wd5.myworkdayjobs.com/REC_RTX_Ext_Gateway/job/US-AZ-TUCSON-802--1151-E-Hermans-Rd--BLDG-802/Naval-Standard-Missile-Systems--NSMS----Principal-Program-Controls-Specialist_01837908 - Excerpt: Naval Standard Missile Systems (NSMS) - Principal Program Controls Specialist US-AZ-TUCSON-802 ~ 1151 E Hermans Rd ~ BLDG 802 posted: Posted 30+ Days Ago ### Sr Mechanical Engineer - Standard Missile - 2nd Shift - Raytheon Technologies - Location: US-AZ-TUCSON-807 ~ 1151 E Hermans Rd ~ BLDG 807 (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Parental leave: 4 weeks (not source-backed) - Non-birth-parent leave: 4 weeks (not source-backed) - Apply: https://globalhr.wd5.myworkdayjobs.com/REC_RTX_Ext_Gateway/job/US-AZ-TUCSON-807--1151-E-Hermans-Rd--BLDG-807/Sr-Mechanical-Engineer---Standard-Missile---2nd-Shift_01830011 - Excerpt: Sr Mechanical Engineer - Standard Missile - 2nd Shift US-AZ-TUCSON-807 ~ 1151 E Hermans Rd ~ BLDG 807 posted: Posted 30+ Days Ago ### Gage Standards Gage Inspector LG4 - 2nd Shift ( Onsite) - Raytheon Technologies - Location: US-FL-JUPITER-MFG ~ 17900 Beeline Hwy ~ MFG BLDG (onsite) - Salary: Not disclosed - Posted: 2026-05-12 - Parental leave: 4 weeks (not source-backed) - Non-birth-parent leave: 4 weeks (not source-backed) - Apply: https://globalhr.wd5.myworkdayjobs.com/REC_RTX_Ext_Gateway/job/US-FL-JUPITER-MFG--17900-Beeline-Hwy--MFG-BLDG/Gage-Standards-Gage-Inspector-LG4---2nd-Shift---Onsite-_01841408 - Excerpt: Gage Standards Gage Inspector LG4 - 2nd Shift ( Onsite) US-FL-JUPITER-MFG ~ 17900 Beeline Hwy ~ MFG BLDG posted: Posted 30+ Days Ago ### Bus Exp & Plan Advisor - Physical Security Products and Standards - The PNC Financial Services Group, Inc. - Location: 5 Locations (unspecified) - Salary: Not disclosed - Posted: 2026-06-02 - Parental leave: 8 weeks (not source-backed) - Non-birth-parent leave: 8 weeks (not source-backed) - Apply: https://pnc.wd5.myworkdayjobs.com/External/job/PA---Pittsburgh/Bus-Exp---Plan-Advisor---Physical-Security-Products-and-Standards_R212498 - Excerpt: Bus Exp & Plan Advisor - Physical Security Products and Standards 5 Locations posted: Posted 10 Days Ago ### Associate Director - Quality Standards and Continuous Improvement - Regeneron Pharmaceuticals - Location: Uxbridge1 (unspecified) - Salary: Not disclosed - Posted: 2026-06-09 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://regeneron.wd1.myworkdayjobs.com/Careers/job/Uxbridge1/Associate-Director--Quality-Standards-and-Improvement_R47976 - Excerpt: Associate Director - Quality Standards and Continuous Improvement Uxbridge1 posted: Posted 3 Days Ago ### Gage Standards Technician - Weekends - Raytheon Technologies - Location: US-GA-MIDLAND-MPC ~ 8801/8987 Macon Rd ~ BLDG MPC (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Parental leave: 4 weeks (not source-backed) - Non-birth-parent leave: 4 weeks (not source-backed) - Apply: https://globalhr.wd5.myworkdayjobs.com/REC_RTX_Ext_Gateway/job/US-GA-MIDLAND-MPC--88018987-Macon-Rd--BLDG-MPC/Gage-Standards-Technician---Weekends_01837037 - Excerpt: Gage Standards Technician - Weekends US-GA-MIDLAND-MPC ~ 8801/8987 Macon Rd ~ BLDG MPC posted: Posted 30+ Days Ago ### Senior Director Engineering Strategy, Front-End Planning, and Engineering Standards - AbbVie Inc. - Location: North Chicago, IL, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013231956-senior-director-engineering-strategy-front-end-planning-and-engineering-standards - Excerpt: Senior Director Engineering Strategy, Front-End Planning, and Engineering Standards North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Position Summary The Senior Director, Engineering Strategy, Front End Planning, and Standards Governance provides enterprise leadership for early-stage capital planning, engineering standards oversight, and long-range technical strategy. This role is responsible for shaping and governing the engineering framework that enables safe, compliant, cost-effective, and sustainable execution of AbbVie's capital and operational priorities. The Senior Director leads cross-functional collaboration to ensure front end planning is rigorous, engineering standards and SOPs are current and effectively governed, and strategic long-range plans align with business growth, network needs, and operational excellence objectives. Key Responsibilities: Front End Planning: Lead front end planning activities for capital and strategic projects, ensuring scope definition, feasibility assessment, basis of design development, and risk identification are completed with rigor. Partner with business, operations, quality, EHS, validation, supply chain, and finance stakeholders to translate business needs into executable engineering plans. Ensure project concepts are evaluated for technical feasibility, cost, schedule, capacity, sustainability, and lifecycle performance. ### Senior Steam Turbine Control Software Standards & Methods Engineer - GE Vernova - Location: Longmont (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Parental leave: 10 weeks (not source-backed) - Non-birth-parent leave: 10 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://gevernova.wd5.myworkdayjobs.com/Vernova_ExternalSite/job/Longmont/Senior-Steam-Turbine-Control-Software-Standards---Methods-Engineer_R5037626-1 - Excerpt: Senior Steam Turbine Control Software Standards & Methods Engineer Longmont posted: Posted 30+ Days Ago ### Director, Program Management Process and Standards - Regeneron Pharmaceuticals - Location: 2 Locations (unspecified) - Salary: Not disclosed - Posted: 2026-06-08 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://regeneron.wd1.myworkdayjobs.com/Careers/job/Warren/Director--Program-Management-Process-and-Standards_R46277 - Excerpt: Director, Program Management Process and Standards 2 Locations posted: Posted 4 Days Ago ### Grill Cook - (M-F 5:30am - 2pm) - AbbVie Inc. - Location: Mettawa, IL, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013582096-grill-cook-m-f-5-30am-2pm- - Excerpt: Grill Cook - (M-F 5:30am - 2pm) Mettawa, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Position performs as an entry level culinarian, the role may assume prep, grill - lunch or breakfast, deli or entrée line responsibilities within the kitchen. Contribute to operational success by following all standards for sanitation and preparation to ensure that food product is of the highest quality in taste and appearance, while satisfy guest expectations. Responsibilities: Reports to Senior Chef or designated kitchen lead including but not limited to; Sous Chef, catering lead or member of management team. Assists with the preparation of food service for Cafe and catering, could include preparing breakfast or lunch short order grill items, and/or preparing items for full service deli. Maintains consistent, efficient service during peak hours. Cooks and prepares food following approved recipes and production standards. Comfortable handling basic kitchen tools, such as knives and slicing machines. Knows basic kitchen terms and is familiar with standard kitchen equipment. Maintain cleanliness of the work area. Demonstrate a practical understanding of kitchen ### Quality Specialist - Industry Standards Compliance - Baker Hughes - Location: HU-PE-FOT-EAST GATE BUSINESS PARK (unspecified) - Salary: Not disclosed - Posted: 2026-06-08 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 8 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://bakerhughes.wd5.myworkdayjobs.com/BakerHughes/job/HU-PE-FOT-EAST-GATE-BUSINESS-PARK/Quality-Specialist---Industry-Standards-Compliance_R164308 - Excerpt: Quality Specialist - Industry Standards Compliance HU-PE-FOT-EAST GATE BUSINESS PARK posted: Posted 4 Days Ago ### Operations Specialist - AbbVie Inc. - Location: Bogotá, Bogota, Colombia (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013578346-operations-specialist - Excerpt: Operations Specialist Bogotá, Bogota, Colombia Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The Operations Specialist is responsible for ensuring the efficient execution, control, and continuous improvement of key finance operations processes within the Shared Service Center, including Concur, P2P, fleet management, employee benefits, and related service activities. This role ensures compliance with internal policies, local regulations, global standards, and service level agreements, while driving operational excellence, stakeholder alignment, and process improvement across the function. Qualifications: Define, document, and maintain standard operating procedures for finance operations processes within the service center. Manage end-to-end processes ensuring accuracy, timeliness, compliance, and adherence to approved workflows and SLAs. Oversee Concur processes, ensuring expense reports and credit card transactions are resolved in accordance with global and local compliance standards. Manage P2P processes, including monitoring blocked invoices, open PO aging, and required follow-up actions. Ensure fleet management processes comply with global standards, local regulations, and internal policies. Monitor vehicle inventory, documentation, taxes, maintenance schedules, and logbook records on a monthly basis. Establish and maintain internal controls to ensure governance, compliance, and ### Sr. Global MES Engineer - AbbVie Inc. - Location: Campoverde, Lazio, Italy (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013576416-sr-global-mes-engineer - Excerpt: Sr. Global MES Engineer Campoverde, Lazio, Italy Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The Senior MES Engineer will design, implement, and optimize Manufacturing Execution System (MES) solutions across AbbVie's global manufacturing network, directly supporting the MES COE Lead's strategic vision for digital transformation and operational excellence. Key Responsibilities: Collaborate with the MES COE Lead and cross-functional teams to deliver high-quality MES solutions aligned with enterprise strategy and standards. Lead technical design, configuration, integration, and testing of MES applications for multiple manufacturing modalities and sites. Develop, document, and maintain MES best practices, playbooks, and standard operating procedures (SOPs). Lead Communities of Practice (COP) meetings across AbbVie's processes and Champion template standardization and process simplification using advanced MES capabilities. Provide technical leadership and mentorship to MES engineers and collaborators. Support Adoption of New MES technology and digital transformation initiatives at the site and network levels. Analyse manufacturing processes and data to identify areas for MES-driven process improvement, automation, and harmonization. Ensure compliance with cGMP, regulatory requirements, and AbbVie's ways of working in all MES engineering activities. ### Lead Engineer - Technical Regulations & Standards - GE Vernova - Location: Greenville (unspecified) - Salary: Not disclosed - Posted: 2026-05-13 - Parental leave: 10 weeks (not source-backed) - Non-birth-parent leave: 10 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://gevernova.wd5.myworkdayjobs.com/Vernova_ExternalSite/job/Greenville/Lead-Engineer---Technical-Regulations---Standards_R5035595-2 - Excerpt: Lead Engineer - Technical Regulations & Standards Greenville posted: Posted 30 Days Ago ### Validation Engineer II (Cleaning) - AbbVie Inc. - Location: Singapore, , Singapore (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013292726-validation-engineer-ii-cleaning- - Excerpt: Validation Engineer II (Cleaning) Singapore, , Singapore Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Purpose: Responsible for adhering to Cleaning Validation Master Plans and strategies for initial and periodic re-validation. Responsible for ensuring risk based cleaning validation policies and standards have robust quality oversight and are in compliance to GMP standards and AbbVie policies and procedures. Major Responsibilities: Adhere to appropriate validation master plans, validation execution plans, and procedures related to risk based cleaning validation of equipment and processes in the AbbVie Operations Campus in Tuas, Singapore comprising of both API and Biologics manufacturing facilities. Generate, execute, and review protocols for initial and subsequent re-qualification programs related to cleaning verification / validation to ensure equipment and cleaning processes are maintained in a validated state. Support the development of specifications and strategies for equipment and processes from a cleanability perspective to ensure equipment qualification and maintenance is in line with the cleaning strategy. Coordinate risk based cleaning validation activities and actively ensure flawless execution of protocols and procedures. Support the Subject Matter Expert (SME) for risk ### Laboratory Technician - AbbVie Inc. - Location: Westport, MO, Ireland (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013573816-laboratory-technician - Excerpt: Laboratory Technician Westport, MO, Ireland Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Execute analysis of raw materials, in-process material, and finished product in compliance with schedule. Complete analysis in accordance with SOP and standard methods. Maintain and comply with Laboratory Documentation and Computerized Systems Data Integrity requirements. Understand Regulations and business processes required to maintain Laboratory Data Integrity. Responsible for the timely completion of chemical testing. Ensure that all test equipment is used and maintained correctly. Raise change requests and data verification as assigned. Ensure all in-process sampling and testing is completed on time. Maintain up-to-date, complete, and precise records of all tests performed. Adhere to cGMP and GLP requirements. Assist in the resolution of quality problems as required. Participation in investigations into failures, out of trends and out of specifications as required. Develop in-house laboratory procedures as appropriate. Support the transfer of new products. Adhere to and supports all EHS standards, procedures, and policies. Keep work area clean and tidy, participation in the 6S program. Qualifications: Degree in an analytical science/biochemistry/toxicology is preferred. Experience ### Senior Engineer – Technical Regulations and Standards - GE Vernova - Location: 3 Locations (unspecified) - Salary: Not disclosed - Posted: 2026-06-02 - Parental leave: 10 weeks (not source-backed) - Non-birth-parent leave: 10 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://gevernova.wd5.myworkdayjobs.com/Vernova_ExternalSite/job/Greenville/Senior-Engineer---Technical-Regulations-and-Standards_R5043175 - Excerpt: Senior Engineer – Technical Regulations and Standards 3 Locations posted: Posted 10 Days Ago ### Senior Manufacturing Execution Systems (MES) Engineer - AbbVie Inc. - Location: Worcester, MA, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012949587-senior-manufacturing-execution-systems-mes-engineer - Excerpt: Senior Manufacturing Execution Systems (MES) Engineer Worcester, MA, United States Company Description: AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on X , Facebook , Instagram , YouTube , LinkedIn and Tik Tok . Job Description: The Manufacturing Execution Systems Engineer will design, implement, and optimize Manufacturing Execution System (MES) solutions across AbbVie's global manufacturing network, directly supporting the MES COE Lead's strategic vision for digital transformation and operational excellence. Responsibilities Collaborate with the Manager, MES and cross-functional teams to deliver high-quality MES solutions aligned with enterprise strategy and standards. Lead technical design, configuration, integration, and testing of MES applications for multiple manufacturing modalities and sites Develop, document, and maintain MES best practices, playbooks, and standard operating procedures (SOPs). Lead Communities of Practice (COP) meetings across AbbVie's processes and Champion template standardization and process simplification using advanced MES capabilities. Provide technical leadership and mentorship to MES engineers and collaborators. Support Adoption of New MES technology and digital transformation initiatives at the site and network levels. Analyze manufacturing processes and data to identify areas for MES-driven process improvement, automation, and harmonization. Ensure compliance with cGMP, regulatory requirements, and AbbVie's ways ### UD Tampoprint Operator - AbbVie Inc. - Location: Westport, MO, Ireland (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012851626-ud-tampoprint-operator - Excerpt: UD Tampoprint Operator Westport, MO, Ireland Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Operate Tampoprint machines in accordance with all GMP and site safety guidelines. Ensure all lab samples are taken and delivered to the ATL Comply with the company standard for attendance and punctuality. Ensure the quality of product/service is to a high standard and adheres to company policy on Quality awareness Assist with training of new employee when required. Maintain regular communication between the Unit Dose Filling Department and Tampoprint area. Reporting of any quality and safety concerns to management Qualifications: Basic knowledge of Tampoprint Machines Basic Computer Skills Excellent communication skills A Keen eye for detail Good documentation skills High level of professionalism and focus on the job Additional Information: AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html ### Associate Technician, Stability - AbbVie Inc. - Location: North Chicago, IL, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013483066-associate-technician-stability - Excerpt: Associate Technician, Stability North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Support the Stability Program to assure studies are place in chambers and that samples are dispensed accurately and in a timely manner. Support the Reference Standard Program to ensure standards are stored, inventoried and dispensed in an accurate and timely manner. Ship samples domestically and international following requirements for shipping dangerous goods and/or controlled substances. Accurately, legibly and contemporaneously document these activities following current Good Manufacturing Practice guidelines and applicable procedures. Perform and verify visual inspections of reserve samples as part of complaint investigations, annual product reviews or other exception events. Maintain a neat and orderly work environment in a continuously audit ready. Responsibilities Dispense stability samples and reference standards from storage and deliver them to local testing laboratories or ship samples domestically and internationally, coordinating with Global Trade Compliance, the recipient and the shipping vendor to ensure all documentation such as invoices are completed correctly to prevent customs delays. Maintain inventory of stability materials, reserve samples and reference standards, ### Director II, Clinical Field Excellence - AbbVie Inc. - Location: Marlow, England, United Kingdom (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013468116-director-ii-clinical-field-excellence - Excerpt: Director II, Clinical Field Excellence Marlow, England, United Kingdom Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Director II, Clinical Field Excellence steers the strategic direction and elevates the performance of Clinical Site Management (CSM)'s clinical field activities globally, driving continuous innovation and improvement, ensuring that AbbVie remains at the forefront of the industry. This individual will foster a culture of excellence in the field, ensuring that the organization's clinical field operations are aligned with best practices and industry standards. This position reports to the Senior Director, Head of Clinical Field Excellence and Site Centricity. This role will collaborate with key cross-functional stakeholders including but not limited to the CSM Leadership Team, Medical Affairs globally, Business Insights/Study Feasibility/Patient Recruitment, Global, Area & Country CSM teams, and CDO stakeholders to achieve and drive the vision. Responsibilities Leadership and Vision : Lead and inspire the Clinical Field Excellence team (direct reports) as well as influence global field teams, fostering a culture of innovation and continuous improvement to achieve industry-leading standards and results. Establish and articulate a strategic vision ### Senior EDC Lead - AbbVie Inc. - Location: Florham Park, NJ, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013495058-senior-edc-lead - Excerpt: Senior EDC Lead Florham Park, NJ, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Purpose: AbbVie Data Science is the best-in-class team within its cross-industry peer group and is responsible for bringing people, process, and technology together to generate business value from clinical trials data. Our operational model is exemplified through execution and innovation. This role is key to ensuring successful delivery against the program- and study-level accountabilities assigned to Clinical Data Strategy Organization. Responsibilities: •Actively participates in the development of common data standards and ensures systems designs comply with the standards, as well as with associated protocol requirements. Ensures that the design team utilizes standards •Establishes and maintains methodology used by the team to design and develop clinical trial systems, benchmarking against industry standards. Ensures that systems are specified to optimize on functionality, end user experience, and data flow. Ensures that the design team meets these expectations •Ensures that TA- and program-level consistency is achieved by the design team •Accountable for the on-time design and delivery of new clinical systems, integrations between systems, ### Senior Receivables Analyst - AbbVie Inc. - Location: North Chicago, IL, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013560806--senior-receivables-analyst - Excerpt: Senior Receivables Analyst North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Purpose: The primary focus of this position is to provide support to the Finance Shared Services (FSS) US Credit & Collection (C&C) team for US: Therapeutics, PCYC, R&D, Aesthetics, and Manufacturing sites. AbbVie operates standardized global processes supported by one ERP system (SAP). Our C&C Mission: We are committed to providing accurate, timely collection and cash application services while managing customer default risk through effective strategy, analysis, negotiations and dispute resolution. Finance Shared Services (FSS) is AbbVie's standardized global end-to-end back-office processes that support operations and transactional business activities enabling our company to run. These standardized processes are our Global Operating Model. Many people refer to FSS as "back-office". Senior analyst role reporting to the Senior Manager of Credit and Collections, US Accounts Receivable. The area of responsibility is managing collections for a portion of the US net sales of approximately $51B and 427,000 customers. Primary Job function: The Senior Receivables Analyst manages the US Financial Shared Services (FSS) Accounts ### Facilities Supervisor - Accendra Health INC - Location: Richmond, VA (unspecified) - Salary: $75K-$80K - Posted: 2026-05-12 - Parental leave: 3 weeks (not source-backed) - Non-birth-parent leave: 3 weeks (not source-backed) - Apply: https://owensminor.wd1.myworkdayjobs.com/OMCareers/job/Richmond-VA/Facilities-Supervisor_REQ_26_30470 - Excerpt: Facilities Supervisor Richmond, VA At Accendra Health, we understand that healthcare is complex, and we're here to make it easier. We help deliver care beyond traditional settings, making essential products and services more accessible through every stage of life. As part of the care team, our teammates play a critical role in delivering personalized, long-term care for the patients we serve. With deep expertise promoting health outside the hospital and a presence in communities nationwide through our Apria and Byram Healthcare brands, Accendra Health does more than just deliver the essentials. If you're interested in meaningful work with impact, explore our career opportunities and join us in our purpose of Bringing Care To Life™. The anticipated salary range for this position is $75k - $80k annual. The actual compensation offered may vary based on job related factors such as experience, skills, education and location. Position Summary The Facilities Supervisor plays a critical role in the safety, functionality, and regulatory compliance of more than 250 locations across the United States. This role is responsible for the day-to-day operation, upkeep, and readiness of the company's facilities, ensuring a safe, functional, and professional environment that supports business operations, customers, and internal teams. This role provides leadership across facility operations, vendor management, space planning, and continuous improvement while maintaining compliance with safety, quality, and regulatory standards. Key Responsibilities Oversee daily facility operations, ensuring buildings, grounds, and shared spaces are maintained to a high standard. Review lease requirements with local leadership to confirm facilities maintenance ### Aseptic Shift Team Lead - AbbVie Inc. - Location: Waco, TX, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013401106-aseptic-shift-team-lead - Excerpt: Aseptic Shift Team Lead Waco, TX, United States Company Description: This is a MD Fill: B2 Night Shift 6pm-6:30am Wednesday - Friday & every other Saturday About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: This is a MD Fill: B2 Night Shift 6pm-6:30am Wednesday - Friday & every other Saturday Responsible for the daily coordination of the production activities in the Multi Dose Aseptic area with responsibility to maintain environmental standards established for Multi Dose Aseptic Areas to ensure regulatory compliance in accordance with Good Manufacturing Practices (GMP's) and department Standard Operating Procedures (SOP's). Responsibilities Accountable for assigned production lines Labor Utilization, Material Loss, Safety. Perform real time document review, facilitate labor by coordinating/ facilitating breaks and line turns, and ensure materials for subsequent batches are available. Coordinates, writes and/or circulates for approval all documentation applicable to the production of filled products that are manufactured, packaged, tested and inspected in compliance with Standard Operating Procedures and current Good Manufacturing Practices. Developing trend lines and conducting data analyses of production issues related to effective and efficient operation of production ### Part Time Specimen Processor I - Myriad Genetics INC - Location: San Diego, CA, United States (unspecified) - Salary: Not disclosed - Posted: 2026-04-29 - Parental leave: 2 weeks (not source-backed) - Non-birth-parent leave: 2 weeks (not source-backed) - Apply: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6130 - Excerpt: Part Time Specimen Processor I San Diego, CA, United States Overview A Specimen Processor I prepares and handles specimens received for testing. Specimen Processors will work with management and quality team members to ensure laboratory activities are defined, documented, and completed to support inspection readiness. They will also ensure compliance is maintained through procedures, training, and documentation. Responsibility Works under the direct supervision of an employee or supervisor who is trained and competent in all relative procedures and processes pertaining to accessioning as well as other assigned processes. Prepares and handles specimens for testing: Assigns specimens an internal tracking number (accession ID). Compares and verifies identifiers on specimens match test order. Ensures specimens are labeled appropriately. Communicates important information pertaining to testing. Looks for and documents problems with specimens. Scans, files, and electronically saves paperwork received with specimens. Files and temporary stores specimens until test release. Transports specimens to testing labs. Packages specimens for return, or external/internal lab send out. Performs other duties as assigned. Complies with and maintains competency in all assigned laboratory policies and procedures. Observes all compliance and regulatory requirements, particularly those associated to data security and patient confidentiality. Actively participates in and maintains accepted laboratory standards for continuing education. Maintains ethical standards in the performance of testing and in interactions with co-workers and other staff. Plays an active role within the team and helps to create a positive work environment. This includes participating in team building events and communicating positively with others. Arrives to work on ### Cost Analyst - AbbVie Inc. - Location: North Chicago, IL, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013160976-cost-analyst - Excerpt: Cost Analyst North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The Newly formed Packaging Region in Internal Manufacturing includes 4 critical manufacturing sites. These sites package nearly all of AbbVie's key products, including Skyrizi, Ubrelvy, Rinvoq, Venetoclax, and Vyalev. This role will function as a shared resource across the Packaging region with a focus on AP16 & Cincinnati sites. The role will lead process improvement initiatives including the implementation and maintenance of regional reporting in Wdesk, drive standardization & consistent accounting treatment across sites. This role will also get the opportunity to gain direct cost accounting & business support experience through working with the Site and Assistant Controllers for AP16 & Cincinnati. The Analyst, Finance is responsible for driving process improvements, consolidation, cost allocation, and collection of data and preparation of reports that maintain AbbVie's cost accounting systems for businesses supported. Responsibilities Serves as a shared resource across the Packaging Region, providing financial support to multiple sites and ensuring alignment of processes and reporting. Leads standardization efforts across the packaging Region, ### Solution COE - Strategy & Operations Senior Director - Salesforce - Location: India - Bangalore (unspecified) - Salary: Not disclosed - Posted: 2026-06-05 - Parental leave: 26 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://careers.salesforce.com/en/jobs/jr344178/solution-coe-strategy-operations-senior-director/ - Excerpt: Solution COE - Strategy & Operations Senior Director India - Bangalore COE - Strategy & Operations Lead Role Description Salesforce Professional Services is building a centralized CoE to standardize how deals are scoped, estimated, and delivered globally. This role is responsible for running the CoE as a measurable, high-performing system. You will ensure: The CoE roadmap is executed The field is adopting the model The impact of the CoE is clearly measured and visible You are not building the model or tools-you are ensuring they are used, tracked, and continuously improved at scale. What You Will Do - Core Responsibilities 1. Own COE Program Management, Performance & Reporting Build and manage dashboards to track: Adoption of CoE standards Usage of tools and agents Deal cycle time improvements Margin and quality impact Provide clear, regular reporting to leadership 2. Measure Field Penetration Track how widely CoE standards and tools are used across: Regions (AMER, EMEA, APAC) P&Ls Product lines Identify gaps in adoption Drive actions to improve penetration 3. Run the CoE Operating Model Manage the CoE roadmap and priorities Track execution across all CoE initiatives Ensure alignment between: Standards Tools Field adoption 4. Manage Knowledge Lifecycle Ensure playbooks, templates, and standards are: Up to date Easy to find Used by the field Turn delivery learnings into updated standards 5. Capture and Drive Continuous Improvement Collect feedback from the field and delivery teams Identify patterns and recurring issues Feed insights back into: Standards (Global Standardization Lead) Tools (Global Tools Lead) 6. ### Solution Advisor Senior Specialist - SAP - Location: Country USA | Internal Posting Location Newtown Square (remote) - Salary: $140K-$262K - Posted: 2026-06-12 - Parental leave: 6 weeks (not source-backed) - Non-birth-parent leave: 6 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.sap.com/job/Newtown-Square-Solution-Advisor-Senior-Specialist-PA-19073/1401825433/ - Excerpt: Solution Advisor Senior Specialist Country USA | Internal Posting Location Newtown Square Requisition ID: 452897 Work Area Sales Expected Travel 0 - 20% Career Status Professional Employment Type Regular Full Time Original Posting Date: 06/08/26 Job Title: Solution Advisor Senior Specialist Location: Newtown Square, PA Work Model: Full Remote Purpose and Objective: SAP America, Inc. seeks a Solution Advisor Senior Specialist at our Newtown Square, PA location to drive customer success and revenue growth by aligning SAP solutions with customer needs, fostering early engagement, and delivering impactful experiences that maximize customer value and ensure high renewal rates. Expectations and Tasks: Engage customers early in the sales cycle, matching needs to SAP solutions, and advising account teams on opportunities based on success probabilities and strategic account positions. Responsible for sales presentations and product demonstrations pre-sales and post-sales. Deliver, help develop, and maintain standard product demonstrations and materials to secure business and increase revenue. Develop and deliver compelling stories and demonstrations that illustrate differentiated business outcomes, utilizing standard messaging and digital assets throughout the customer journey. Collaborate with customers and partners to co-create an agreed-upon SAP vision, aligning messaging and gaining customer trust. Ensure world-class customer experiences in critical segments, driving adoption and consumption to maximize customer value. Continuously explore and communicate the added val ### Senior Clinical Research Associate - AbbVie Inc. - Location: Bucharest, Bucharest, Romania (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012592216-senior-clinical-research-associate - Excerpt: Senior Clinical Research Associate Bucharest, Bucharest, Romania Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Considered as the Primary Sponsor Point of contact for the investigative site. Advanced level of competency or experience in providing contextual information on the clinical trials, connecting stakeholders to the investigative sites and strengthening Abbvie's positioning. Ability to motivate and align monitoring community through leadership and mentorship. Aligns, trains and motivates the site staff and principal investigator on the goals of the clinical trial program, protocol, and patient treatment principles for the trial ensuring a trusted partnership. Able to support, guide, and mentor junior personnel on Site Management activities. Conducts site evaluation, site training, routine on-site and off-site monitoring, and site closure monitoring activities with compliance to the protocol and monitoring plans, in accordance with applicable regulations, Good Clinical Practices (GCPs), ICH Guidelines, AbbVie Standard Operating Procedures (SOPs), and quality standards, ensuring safety and protection of study subjects. Superior understanding of site engagement and ability to customize site engagement strategy for assigned study/ies and critically apply new strategies as needed. Gather ### Manufacturing Support Engineer II -temporary 6 months - AbbVie Inc. - Location: Heredia, Heredia Province, Costa Rica (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013519766-manufacturing-support-engineer-ii-temporary-6-months - Excerpt: Manufacturing Support Engineer II -temporary 6 months Heredia, Heredia Province, Costa Rica Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: PURPOSE STATEMENT Maintain and optimize the operation of existing products, processes, and systems, ensuring their sustainability, efficiency, and reliability throughout their life cycle. This will be achieved through the application of best practices in project management and operational excellence, ensuring compliance with applicable procedures and regulations. MAJOR RESPONSIBILITIES Identify and implement methods, workstations, and plant layouts that ensure quality, productivity, and optimal environment, health, and safety conditions so that the manufacturing process meets key business goals. Carry out waste analysis to achieve the optimal value of processes and generate savings aligned with plant goals. Define, approve, update, and manage production standards for each manufacturing process operation in order to optimize human resource use (headcount). Likewise, assess the impact on approved standards due to process changes and/or new operations or products. Guide continuous improvement teams (SWAT, Lean thinkers) in root cause analysis through the application of Opex tools. Serve as a facilitator in the implementation of improvements ### Senior Manager, Inventory Control - AbbVie Inc. - Location: Westport, MO, Ireland (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012481411-senior-manager-inventory-control- - Excerpt: Senior Manager, Inventory Control Westport, MO, Ireland Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: AbbVie Ireland is seeking a Senior Manager, Inventory Control to oversee all aspects of inventory management for both Pharma and Biologics manufacturing at our site in Westport. Reporting to the Director of Supply Chain and supervising a team of three, this leadership role is accountable for ensuring compliance with all cGMP regulatory and financial requirements for material handling, storage, and achieving yearly budgetary targets. The Senior Manager will work closely with cross-functional teams to maintain high-quality standards and drive strategic improvements in inventory processes. Responsibilities: Manage, motivate, and develop the Inventory Control team through effective communication, performance reviews, coaching, and Individual Development Plans (IDPs). Oversee all Site Inventory management processes, ensuring inventory levels, consignment stocks, and Material Review Board management are aligned with Site goals and metrics. Define and implement site inventory policies and procedures to ensure compliance with cGMP, Quality, EHS, FDA, HPRA, and SOX requirements. Maintain oversight of SAP and S4 systems, ensuring alignment with AbbVie standards and implementation ### Senior Technical Analytical Specialist - AbbVie Inc. - Location: Sligo, SO, Ireland (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013557936-senior-technical-analytical-specialist - Excerpt: Senior Technical Analytical Specialist Sligo, SO, Ireland Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on X , Facebook , Instagram , YouTube , LinkedIn and Tik Tok . Job Description: We are looking for a Senior Technical Analytical Specialist to join our Technical Operations Team, at our Active Pharmaceutical Ingredients manufacturing site in Sligo . The successful candidate will be the the primary technical authority for analytical laboratory operations across routine and advanced testing, with accountability for compliance, verification, laboratory infrastructure, and support for the new laboratory. The role combines technical stewardship with laboratory coordination to ensure analytical activities, documentation, equipment, and systems consistently meet or exceed regulatory, quality, and safety standards. Role and Responsibilities Provide analytical testing and technical support for routine, non-routine, and advanced applications, ensuring testing meets product, safety, and quality requirements. Lead compliance verification for analytical results, methods, equipment, records, and data to ensure alignment with internal standards and external requirements, including cGMP, GLP, ICH, FDA/HPRA, and EHS. Author, update, and maintain SOPs, protocols, and technical records to support audit readiness and regulatory compliance. Oversee laboratory infrastructure, including asset management, ### Sr. Equipment Engineer - Intuitive Surgical, Inc. - Location: Mexicali, , Mexico (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Parental leave: 8 weeks (not source-backed) - Non-birth-parent leave: 8 weeks (not source-backed) - Apply: https://jobs.smartrecruiters.com/Intuitive/744000126122279-sr-equipment-engineer - Excerpt: Sr. Equipment Engineer Mexicali, , Mexico Company Description: It started with a simple idea: what if surgery could be less invasive and recovery less painful? Nearly 30 years later, that question still fuels everything we do at Intuitive . As a global leader in robotic-assisted surgery and minimally invasive care , our technologies-like the da Vinci surgical system and Ion -have transformed how care is delivered for millions of patients worldwide. We're a team of engineers, clinicians, and innovators united by one purpose: to make surgery smarter, safer, and more human. Every day, our work helps care teams perform with greater precision and patients recover faster, improving outcomes around the world. The problems we solve demand creativity, rigor, and collaboration. The work is challenging, but deeply meaningful-because every improvement we make has the potential to change a life. If you're ready to contribute to something bigger than yourself and help transform the future of healthcare , you'll find your purpose here. Job Description: Primary Function of Position: The Senior Equipment Engineer is responsible for designing, developing, validating, and maintaining manufacturing equipment to ensure efficient, compliant, and high-quality production of medical devices. This role drives continuous improvement initiatives using Six Sigma methodologies, establishes equipment standards, and provides technical leadership, including mentoring junior team members. Essential Job Duties Lead the design, specification, and procurement of new manufacturing equipment and tooling. Develop and maintain equipment standards and documentation for consistency and compliance. Apply Six Sigma principles (DMAIC, SPC, root cause analysis) to optimize ### Senior Assistant, Catering (M-F 8am-4:30pm) - AbbVie Inc. - Location: North Chicago, IL, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012931926-senior-assistant-catering-m-f-8am-4-30pm- - Excerpt: Senior Assistant, Catering (M-F 8am-4:30pm) North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: As a member of the Foodservice Team, you are responsible for being a strong team player, taking initiative and assisting others as needed to ensure excellent guest service. This role supports Foodservice Management and is responsible for all aspects of the catering floor, including the executive suite. The ideal candidate will have catering and cooking experience, be highly organized, and be able to multitask effectively in a fast-paced environment. Responsibilities Support Foodservice Management by coordinating and overseeing daily catering and foodservice operations, including the executive suite. Provide leadership to catering floor staff through training, coaching, work direction, and daily operational support. Ensure team members have the tools, equipment, and resources needed to carry out daily production effectively. Maintain compliance with established policies, procedures, and quality standards related to sanitation, safety, recipes, and portion control. Prepare and oversee catering menu production to ensure items are completed accurately and according to standardized recipes. Coordinate catering activities and communicate operational needs ### Operations Leader (OSD Manufacturing) - AbbVie Inc. - Location: Sligo, SO, Ireland (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012354207-operations-leader-osd-manufacturing- - Excerpt: Operations Leader (OSD Manufacturing) Sligo, SO, Ireland Company Description: About AbbVie: AbbVie is a global, research-driven biopharmaceutical company committed to developing innovative medicines and delivering excellence in pharmaceutical manufacturing. Job Description: As the Operations Leader, you will lead the production of high-quality pharmaceutical drug products in a dynamic and regulated environment. You will ensure your team consistently delivers on operational objectives, compliance standards, safety, and continuous improvement initiatives. This is a highly visible and rewarding leadership role for individuals committed to quality and operational excellence. Key Responsibilities: Oversee and execute all drug product manufacturing operations, ensuring compliance with internal and external regulatory standards (including cGMP, HPRA/FDA). Provide leadership, direction, and motivation to a team of 8-45, ensuring effective performance, strong communication, and development of team members. Plan staffing and material resources to guarantee smooth, efficient, and safe daily operations. Coordinate onboarding, training, and ongoing skills development for team members. Monitor and manage key performance indicators for the department (e.g., yield, production rate, resource usage, attendance, overtime). Maintain accurate records and timely updates in manufacturing and personnel systems. Foster a culture of safety, quality, innovation, and continuous improvement throughout the manufacturing area. Collaborate with other shift leaders and cross-functional teams to deliver operational results and support site-wide projects. Lead and support facility and equipment/process improvements and Operational Excellence (OpEx) initiatives. Ensure compliance with safety, environmental, and quality SOPs, and manage adherence to all relevant procedures, policies, and regulations. Support HR processes including performance management, annual reviews, and employee relations. Lead the ### WMS Developer II - Accendra Health INC - Location: 3610 Accendra India (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Parental leave: 3 weeks (not source-backed) - Non-birth-parent leave: 3 weeks (not source-backed) - Apply: https://owensminor.wd1.myworkdayjobs.com/OMCareers/job/3610-Accendra-India/WMS-Developer-II_REQ_25_29233 - Excerpt: WMS Developer II 3610 Accendra India At Owens & Minor, we are a critical part of the healthcare process. As a Fortune 500 company with 350+ facilities across the US and 22,000 teammates in over 90 countries, we provide integrated technologies, products and services across the full continuum of care. Customers-and their patients-are at the heart of what we do. Our mission is to empower our customers to advance healthcare, and our success starts with our teammates. RESPONSIBILITIES Works directly with business development teams during project envisioning/inception to devise best solutions and reasonable, accurate time/cost estimates for each project. Contributes to functional and technical application design. Reviews/establishes “best practice” processes and uses case design/reviews. Maintains ability to document and read functional and technical specifications. Helps to define and implement applications development best practices, standards, and processes. Thoroughly documents application development work using established team documentation standards. Self-manages workload and work assignments within an application development team that delivers projects/tasks through a software development life cycle, with an eye toward project timelines and utilization. Performs additional duties as directed. EDUCATION & EXPERIENCE Bachelor's Degree, preferably in related field (Computer Science, Information Technology, etc.) 2 or more years of IT Applications Development experience (.NET, C#, ASP.NET, full-stack development) Experience with ASP.NET MVC / Razor, Entity Framework, WCF, HTML, CSS, JQuery, Ajax, and JSON Or any combination of education and experience to meet the above requirements KNOWLEDGE, SKILLS, & ABILITIES Ability to design and implement databases with SQL Server, Oracle experience preferred Experience ### Specimen Processor I - Myriad Genetics INC - Location: Salt Lake City, UT, United States (unspecified) - Salary: Not disclosed - Posted: 2026-04-29 - Parental leave: 2 weeks (not source-backed) - Non-birth-parent leave: 2 weeks (not source-backed) - Apply: https://ekgn.fa.us6.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX_2001/job/6116 - Excerpt: Specimen Processor I Salt Lake City, UT, United States Overview A Specimen Processor I prepares and handles specimens received for testing. Specimen Processors will work with management and quality team members to ensure laboratory activities are defined, documented, and completed to support inspection readiness. They will also ensure compliance is maintained through procedures, training, and documentation. Shift: Tuesday-Friday 8:00am-4:30pm and Saturday 8:30am-5:00pm Pay: Starting at $18/hr, plus $3/hr on Saturday Responsibility Works under the direct supervision of an employee or supervisor who is trained and competent in all relative procedures and processes pertaining to accessioning as well as other assigned processes. Prepares and handles specimens for testing: Assigns specimens an internal tracking number (accession ID). Compares and verifies identifiers on specimens match test order. Ensures specimens are labeled appropriately. Communicates important information pertaining to testing. Looks for and documents problems with specimens. Scans, files, and electronically saves paperwork received with specimens. Files and temporary stores specimens until test release. Transports specimens to testing labs. Packages specimens for return, or external/internal lab send out. Performs other duties as assigned. Complies with and maintains competency in all assigned laboratory policies and procedures. Observes all compliance and regulatory requirements, particularly those associated to data security and patient confidentiality. Actively participates in and maintains accepted laboratory standards for continuing education. Maintains ethical standards in the performance of testing and in interactions with co-workers and other staff. Plays an active role within the team and helps to create a positive work environment. This includes participating ### Distribution Specialist, Associate - Accendra Health INC - Location: Everett, WA (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Parental leave: 3 weeks (not source-backed) - Non-birth-parent leave: 3 weeks (not source-backed) - Apply: https://owensminor.wd1.myworkdayjobs.com/OMCareers/job/Everett-WA/Distribution-Specialist--Associate_REQ_26_30615 - Excerpt: Distribution Specialist, Associate Everett, WA At Accendra Health, we understand that healthcare is complex, and we're here to make it easier. We help deliver care beyond traditional settings, making essential products and services more accessible through every stage of life. As part of the care team, our teammates play a critical role in delivering personalized, long-term care for the patients we serve. With deep expertise promoting health outside the hospital and a presence in communities nationwide through our Apria and Byram Healthcare brands, Accendra Health does more than just deliver the essentials. If you're interested in meaningful work with impact, explore our career opportunities and join us in our purpose of Bringing Care To Life™. The anticipated pay range for this positions is as follows: $21.00/hr POSITION SUMMARY Performs warehouse tasks within the Byram Healthcare Distribution Centers in a safe, accurate and timely manner. Primarily responsible for pulling, packaging and shipping customer orders of healthcare supplies. Unloads, receives, and processes inbound shipments. Performs bin replenishment, moves product around the distribution centers to endure efficient processing, and prepares pick locations. Accurately picks, packs, sorts and loads outbound products in accordance with customer specifications. RESPONSIBILITIES (Exclude if less than 15%) Meet daily minimum productivity numbers for pulling and packing/shipping Process daily orders in a timely and accurate manner according to department standards in a pick / pack environment; production rates will vary per site: 18-30 orders per hour on average Always maintain productivity and quality standards Follows general sequencing and process procedures ### Supervisor, Internal Audit - AbbVie Inc. - Location: North Chicago, IL, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012922961-supervisor-internal-audit - Excerpt: Supervisor, Internal Audit North Chicago, IL, United States Company Description: AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on X , Facebook , Instagram , YouTube , LinkedIn and Tik Tok . Job Description: The Supervisor, Internal Audit is responsible for supporting and at times leading strategic Internal Audit initiatives with a focus on strategic projects, such as the annual Internal Audit (IA) risk assessment, ensuring compliance with Institute of Internal Auditors (IIA) standards, and supporting the Director with third‑party audits. The position engages with stakeholders across the business to gather and assess internal documentation related to third‑party relationships and coordinates with external consultants to support effective audit execution across all phases of third‑party audits. This role strengthens the company's ability to create, protect, and sustain value by providing independent, objective assurance and insight into the effectiveness of governance, risk management, and internal control processes related to third‑party relationships and other key risk areas. Responsibilities Support and enhance third‑party audit activities Designs and enhances internal processes for gathering data and building insights to inform third‑party audits, including standardized approaches for collecting, organizing, and analyzing information on third‑party relationships. Develops ### Sr. Director, Global Network & Network Security - AbbVie Inc. - Location: North Chicago, IL, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013307436-sr-director-global-network-network-security - Excerpt: Sr. Director, Global Network & Network Security North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The Senior Director will provide senior leadership to create and execute Global Network, Voice and Network Security strategies that support AbbVie business goals. This role owns the end-to-end direction and performance of AbbVie's Data Network, Voice Network, and Network Security capabilities worldwide, with enterprise-wide impact and influence. This role will build collaborative partnerships with technology and functional domain vice presidents and key business stakeholders. Lead delivery of secure, reliable, and scalable network services and security controls that address prioritized business problems, support innovation, and enable global growth. Objectives are defined in collaboration with senior AbbVie leadership and results are assessed from a 3-5 year perspective. Responsibilities Global Strategy & Roadmap: Define and lead the 3-5 year global strategy and roadmap for Data Network, Voice Network, and Network Security to enable AbbVie's business priorities, digital transformation, and growth. Network Architecture & Standards: Partner with Enterprise Architecture to establish global reference architectures, engineering standards, and design patterns for ### QA Digital Compliance Manager - AbbVie Inc. - Location: Campoverde, Lazio, Italy (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013488226-qa-digital-compliance-manager - Excerpt: QA Digital Compliance Manager Campoverde, Lazio, Italy Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The QA Digital Compliance Manager is responsible for ensuring that all digital systems, records, instruments, processes and data handling within operations adhere to relevant regulatory, legal, best practices and industry standards. Key Responsibilities: Monitoring and ensuring adherence to relevant regulatory bodies (e.g. FDA, EMA) for digital content and initiatives in compliance with regulations like FDA 21 CFR Part 11 and EU Annex 11. Keeping updating with evolving digital compliance regulations and trends (eg Annex 22 about AI). Ensuring and maintaining Quality oversight of data integrity and traceability across computerized systems lifecycle such as manufacturing execution system, and laboratory information management systems (LIMS), electronic lab notebooks (ELN/LES), and instrument software. Support the implementation of proper cybersecurity measures to protect data and prevent unauthorized access or tampering. Supporting as Subject Matter Expert the training to employees and stakeholders on digital compliance requirements and best practices and the audit of digital systems and assure the adherence to GMP, company policies and other relevant standards, ### SAP Customer Master Data & Analytics - AbbVie Inc. - Location: North Chicago, IL, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012925349-sap-customer-master-data-analytics - Excerpt: SAP Customer Master Data & Analytics North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The Customer Master Data & Analytics Analyst , within the Finance Shared Services (FSS) organization, supports the Order to Cash (OTC) process by executing established data governance, data quality, and operational standards for Customer Master Data across SAP S/4HANA and integrated systems. This role works closely with business, finance, and technology stakeholders to ensure customer master data is accurate, compliant, and maintained in a timely manner to support effective OTC execution, regulatory requirements, and reliable reporting. The Master Data Analyst contributes to continuous improvement efforts, supports analytics and reporting activities, and assists in driving process consistency and operational efficiency within the Customer Master Data domain. Key Responsibilities Perform DSP Reviewer activities by validating customer master data for accuracy, completeness, and compliance, reviewing supporting documentation, and approving or rejecting requests in accordance with established governance and OTC process standards. Perform ongoing customer master data maintenance through bulk updates in line with approved governance controls. Participate in global projects ### Senior Manager, Payer & Channel Analytics - Market Access Patient Services - AbbVie Inc. - Location: Mettawa, IL, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012910846-senior-manager-payer-channel-analytics-market-access-patient-services - Excerpt: Senior Manager, Payer & Channel Analytics - Market Access Patient Services Mettawa, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The Market Access Patient Services (MAPS) organization within APEX plays an instrumental role in shaping market access strategies for all of AbbVie's domestic brands. As a member of this team, you will plan and execute standard and ad-hoc analytics to identify/ quantify payer opportunities and threats, make specific recommendations on the development of market access strategies and tactics, develop analytical capabilities, enable organizational learning, and ensure alignment of analytical insights with the broader commercial goals of each brand. The role requires foundational data analytics training and experience in the pharmaceutical or related industry. The role provides insights that directly impact patient and physician access to AbbVie brands through its influence on the development of pricing, contracting and other access strategies. MAJOR RESPONSIBILITIES Lead standard/ ad-hoc analytics on key brands in migraine and psychiatry focused on providing insights that influence market access strategy through data analytics, customer insights and business knowledge. Co-develop with U.S. ### EHS Officer - AbbVie Inc. - Location: Grâce-Hollogne, Wallonia, Belgium (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013555591-ehs-officer - Excerpt: EHS Officer Grâce-Hollogne, Wallonia, Belgium Company Description: AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on X , Facebook , Instagram , YouTube , LinkedIn and Tik Tok . Job Description: AbbVie is seeking an EHS Officer to strengthen the Environmental, Health & Safety culture at our Grâce‑Hollogne production site . In this role, you will promote safe work practices, support continuous improvement initiatives, and help enhance employee well‑being and environmental performance. Acting as a key point of contact in the field, you will ensure that regulatory requirements and AbbVie standards are understood, applied, and continuously improved across all departments. EHS Culture, Training & Awareness Lead EHS prevention campaigns and contribute to Tier and departmental meetings. Deliver EHS training and awareness sessions, including onboarding for new employees. Update and develop EHS training materials and support communication initiatives across the site. Field Presence, Inspections & Observations Conduct regular workplace visits, safety observations, and gemba walks. Perform inspections of construction and maintenance activities to ensure compliance with AbbVie standards and legal requirements. Follow up on positive safety observations and support departments in implementing improvements. Risk Assessment, Incident Investigation & Corrective Actions ### Associate Manager, Payer & Channel Analytics - Market Access Patient Services - AbbVie Inc. - Location: Mettawa, IL, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013503544-associate-manager-payer-channel-analytics-market-access-patient-services - Excerpt: Associate Manager, Payer & Channel Analytics - Market Access Patient Services Mettawa, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The Market Access Patient Services (MAPS) organization within APEX plays an instrumental role in shaping market access strategies for all of AbbVie's domestic brands. As a member of this team, you will plan and execute standard and ad-hoc analytics to identify/ quantify payer opportunities and threats, make specific recommendations on the development of market access strategies and tactics, develop analytical capabilities, enable organizational learning, and ensure alignment of analytical insights with the broader commercial goals of each brand. The role requires foundational data analytics training and experience in the pharmaceutical or related industry. The role provides insights that directly impact patient and physician access to AbbVie brands through its influence on the development of pricing, contracting and other access strategies. MAJOR RESPONSIBILITIES Execute standard / ad-hoc analyses on a key brands focused on providing insights that influence market access strategy through data analytics, customer insights and business knowledge. Assist in the development with ### Mechanical Engineer II - Standard Missile - 2nd Shift - Raytheon Technologies - Location: US-AZ-TUCSON-801 ~ 1151 E Hermans Rd ~ BLDG 801 (External Site) (unspecified) - Salary: Not disclosed - Posted: 2026-05-12 - Parental leave: 4 weeks (not source-backed) - Non-birth-parent leave: 4 weeks (not source-backed) - Apply: https://globalhr.wd5.myworkdayjobs.com/REC_RTX_Ext_Gateway/job/US-AZ-TUCSON-801--1151-E-Hermans-Rd--BLDG-801-External-Site/Mechanical-Engineer-II---Standard-Missile---2nd-Shift_01830126 - Excerpt: Mechanical Engineer II - Standard Missile - 2nd Shift US-AZ-TUCSON-801 ~ 1151 E Hermans Rd ~ BLDG 801 (External Site) posted: Posted 30+ Days Ago ### Lead SAP Customer Master Data & Analytics - AbbVie Inc. - Location: North Chicago, IL, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012905172-lead-sap-customer-master-data-analytics - Excerpt: Lead SAP Customer Master Data & Analytics North Chicago, IL, United States Company Description: AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on X , Facebook , Instagram , YouTube , LinkedIn and Tik Tok . Job Description: The Lead, Customer Master Data & Analytics, within the Finance Shared Services (FSS) organization, supports the Order-to-Cash (OTC) Global Process Lead by ensuring strong governance, data quality, and operational excellence for Customer Master Data across SAP S/4HANA and integrated systems. This role provides people leadership and partners cross-functionally to deliver accurate, compliant, and timely customer data that enables effective OTC execution, regulatory compliance, and data-driven decision-making, while driving continuous improvement, analytics, and process innovation. Responsibilities Lead the Customer Master Data vision, roadmap, and governance framework across SAP S/4HANA and integrated systems. Serve as the senior point of contact for Customer Master Data across Customer Service, Supply Chain, Pricing, Finance/AR, Commercial, and IT. Define and enforce global customer data standards, stewardship practices, and data quality controls to ensure accuracy, completeness, and compliance. Drive continuous improvement initiatives across Customer Master Data processes, balancing global standardization with operational agility. Oversee Customer MDM/DSP (Syniti - ### Director, Process Engineering (Peptides) - AbbVie Inc. - Location: North Chicago, IL, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012925336-director-process-engineering-peptides- - Excerpt: Director, Process Engineering (Peptides) North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Purpose: The Director of Process Engineering will lead the process engineering effort for multiple strategic projects. This role serves as the owner-side Design Authority for process engineering on major biopharmaceutical capital programs. This role provides strategic leadership, technical governance, and oversight of all process engineering activities supporting large-scale manufacturing facility projects. The incumbent is responsible for ensuring that process systems are designed, integrated, and implemented in alignment with corporate engineering standards, regulatory expectations, and operational requirements. The role provides technical oversight of A&E contractor engineering activities and ensures that core process engineering deliverables-including process flow diagrams (PFDs), piping and instrumentation diagrams (P&IDs), cause and effect diagrams, process schematics, and operations philosophy documentation-meet the technical, safety, and operational standards required for pharmaceutical manufacturing facilities. As part of the project leadership team, the Director ensures effective integration of process design with utilities, automation, commissioning, qualification, and operational readiness activities. The role also supports corporate capital governance stage-gate processes, process safety management, ### Study Project Manager (Medical Affairs/Immunology/Oncology) - AbbVie Inc. - Location: Mettawa, IL, United States (unspecified) - Salary: $148K-$202K - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013120726-study-project-manager-medical-affairs-immunology-oncology- - Excerpt: Study Project Manager (Medical Affairs/Immunology/Oncology) Mettawa, IL, United States Company Description: AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on X , Facebook , Instagram , YouTube , LinkedIn and Tik Tok . Job Description: Key Responsibilities Independently lead Medical Affairs + Health Impact (MHI) funded research, including Externally Sponsored Collabs & Non-Interventional Studies (NIS) (single & multi-country) from inception to closure, in compliance with quality standards. Support strategic leadership of the Cross-Functional Team. Drive deliverables & timelines. Lead & manage meetings with stakeholders. Manage vendors, recruitment, CTMS & eTMF. Maintain Inspection Readiness. Identify, mitigate & manage risks. Develop & manage study materials. Provide training to stakeholders. Support EDC, IRT, & ePRO design specifications, user acceptance testing, plans & key risk indicators, & system management activities. Manage IP & study supplies. Support process improvement initiatives & serve as a subject matter expert &/or mentor. Qualifications: Education & Experience Must possess a Master's or foreign education equivalent & 2 years of clinical research work experience. Of work experience required, must have 2 years in each of the following: applying standard quality procedures to MHI research, including SOP, ICH/GCP, Global Regulations; ### Director, Process Engineering - AbbVie Inc. - Location: North Chicago, IL, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013193521-director-process-engineering - Excerpt: Director, Process Engineering North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Purpose: The Director of Process Engineering will lead the process engineering effort for multiple strategic projects. This role serves as the owner-side Design Authority for process engineering on major biopharmaceutical capital programs. This role provides strategic leadership, technical governance, and oversight of all process engineering activities supporting large-scale manufacturing facility projects. The incumbent is responsible for ensuring that process systems are designed, integrated, and implemented in alignment with corporate engineering standards, regulatory expectations, and operational requirements. The role provides technical oversight of A&E contractor engineering activities and ensures that core process engineering deliverables-including process flow diagrams (PFDs), piping and instrumentation diagrams (P&IDs), cause and effect diagrams, process schematics, and operations philosophy documentation-meet the technical, safety, and operational standards required for pharmaceutical manufacturing facilities. As part of the project leadership team, the Director ensures effective integration of process design with utilities, automation, commissioning, qualification, and operational readiness activities. The role also supports corporate capital governance stage-gate processes, process safety management, and ### Pricing & Rebate Manager, APAC Commercial Excellence - Boston Scientific - Location: Penang (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Parental leave: 8 weeks (not source-backed) - Non-birth-parent leave: 8 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.bostonscientific.com/job/Penang-Pricing-&-Rebate-Manager%2C-APAC-Commercial-Excellence/1399280300/ - Excerpt: Pricing & Rebate Manager, APAC Commercial Excellence Penang Purpose Statement The APAC Pricing & Rebates Manager is responsible for driving pricing and rebate policy, process standardization, and governance across APAC markets. The role leads the development, implementation, and continuous improvement of regional pricing frameworks, controls, approval threshold methodologies, and standard operating procedures (SOPs) to support consistent, compliant, and scalable pricing practices across the region. The role partners closely with APAC markets to support the implementation and ongoing maintenance of pricing and rebate policies, local SOPs, governance controls, and pricing processes aligned with regional standards and local market requirements. This includes supporting markets through annual pricing governance reviews, pricing process harmonization, operational readiness activities, and continuous improvement initiatives. In addition, the role supports the implementation, adoption, and governance of pricing and rebate digital tools and enterprise transformation initiatives to strengthen operational effectiveness, transparency, scalability, and pricing governance maturity across APAC. Responsibilities Lead the development, implementation, maintenance, and continuous improvement of APAC pricing and rebate policy. Drive pricing and rebate process standardization and harmonization across APAC markets while balancing policy requirements with local market needs. Partner with market and regional stakeholders to support the development, implemen ### SHEQ Manager | Olleco Bunge (País Vasco o Andalucía) - Bunge - Location: Bilbao (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Parental leave: 6 weeks (not source-backed) - Non-birth-parent leave: 6 weeks (not source-backed) - Apply: https://jobs.bunge.com/job/Bilbao-SHEQ-Manager-Olleco-Bunge-%28Pa%C3%ADs-Vasco-o-Andaluc%C3%ADa%29-BI-48508/1399739733/ - Excerpt: SHEQ Manager | Olleco Bunge (País Vasco o Andalucía) Bilbao Requisition Number: 45912 Olleco Bunge is seeking a SHEQ Manager to join our team in Andalucia or Basque country. Employment will be through Olleco Bunge's local legal entities. JOB PURPOSE To support the delivery of a comprehensive Health, Safety, Environmental and ISCC (International Sustainability and Carbon Certification) service across the business, ensuring full compliance with all applicable legislation and standards. To establish, implement and maintain effective systems and processes that drive company performance in Health & Safety, environmental compliance, ISCC requirements, and continuous improvement. To contribute to the development, implementation and ongoing maintenance of ISO 9001 quality standards. POSITION IN ORGANISATION The position is expected to support local management and the wider SHEQ team in the development of SHEQ Standards. Reports to the SHEQ Director & Business Improvement Director and is a team player, dedicated to supporting the success of the rest of the SHEQ Team. PRINCIPLE ACCOUNTABILITIES Ensuring that all interactions are undertaken in a professional and courteous manner. KEY TASKS Support the development and execution of the Spain SHEQ strategy and chair the monthly SHEQ Board to drive performance and accountability. Produce and analyse monthly SHEQ reports, identifying trends, risks, and areas for improvement. Implement, maintain, and continuously improve SHEQ management systems, ensuring compliance with ISO standards, ISCC requirement ### Director, Data Center Building Automation - Michigan - Oracle - Location: MI, United States, US (onsite) - Salary: $139K-$292K - Posted: 2026-06-03 - Parental leave: 14 weeks (not source-backed) - Non-birth-parent leave: 14 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://careers.oracle.com/en/sites/jobsearch/job/333113/ - Excerpt: Director, Data Center Building Automation - Michigan MI, United States, US This position will be full-time on-site at Oracle's new Michigan AI data center, located in Saline Township, 35 miles southwest of Ann Arbor, Michigan. Relocation assistance may be available in accordance with Oracle's relocation policies. As Director of Building Automation, you will define and govern automation strategy for OCI's global data center portfolio. This role sets standards and long-term direction for building management systems, OT controls architecture, cybersecurity, alarming, integration practices, and analytics that underpin safe, efficient, and scalable operations across the fleet. You will lead managers, senior engineers, and strategic vendor partners responsible for automation platforms and standards across multiple regions. This role balances technical vision and execution discipline, ensuring OCI's building automation ecosystem evolves in a consistent, secure, and operationally effective way as the business scales. You will partner across engineering, facilities, IT, security, construction, commissioning, and product teams to align standards, investment priorities, and system capabilities. Key Responsibilities Lead strategy, governance, and standards for BMS, DCIM, OT controls, and automation systems across OCI's global portfolio. Define long-term controls architecture, alarm philosophy, OT network standards, naming conventions, integration requirements, and supportability expectations across multi-vendor environments. Oversee design, integration, commissioning, and operational handoff of major automation and controls initiatives across new sites, expansions, and retrofit programs. Establish cybersecurity requirements and governance for OT systems in partnership with IT and security teams, including segmentation, access control, remote support methods, device lifecycle management, and compliance practices. Drive adoption of smart ### Principal Data Center Planning and Scheduling Lead - Oracle - Location: United States, US (unspecified) - Salary: $126K-$264K - Posted: 2026-06-01 - Parental leave: 14 weeks (not source-backed) - Non-birth-parent leave: 14 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://careers.oracle.com/en/sites/jobsearch/job/335303/ - Excerpt: Principal Data Center Planning and Scheduling Lead United States, US We are seeking a strategic and operationally strong leader to establish and scale integrated planning and scheduling standards across OCI's global data center delivery portfolio. Operating within the Chief of Staff organization, this role is responsible for developing enterprise-level scheduling governance, standardized planning frameworks, milestone structures, and portfolio-level schedule visibility that enable predictable, scalable delivery across rapidly expanding programs and campuses. This role will partner closely with Program E2E, PMO, Construction Delivery, Long Range Planning, Cost Controls, Design, TPM, and site scheduling teams to drive consistency in how projects are planned, baselined, tracked, escalated, and reported. Key Responsibilities Enterprise Planning & Schedule Governance Develop and maintain enterprise scheduling standards, planning frameworks, and governance processes across OCI construction programs Establish standardized milestone structures, critical path methodologies, schedule maturity expectations, and baseline governance practices Define enterprise expectations for: schedule development schedule updates change management forecasting recovery planning variance reporting Drive consistency in scheduling practices across regions, campuses, and delivery teams Integrated Program & Portfolio Planning Support development of integrated portfolio-level planning frameworks connecting: long range planning design procurement construction commissioning operational readiness Partner with Long Range Planning and Program E2E teams to support pipeline planning and scalable campus delivery sequencing Ensure enterprise-level visibility into major dependencies, sequencing risks, and delivery constraints across the portfolio Schedule Visibility & Executive Reporting Establish portfolio-level schedule health reporting, trend analysis, and milestone visibility frameworks Develop standardized executive reporting structures focused on: milestone attainment critical path risks ### Data Center Integrated Planning & Scheduling Lead - Oracle - Location: United States, US (unspecified) - Salary: $98K-$200K - Posted: 2026-06-01 - Parental leave: 14 weeks (not source-backed) - Non-birth-parent leave: 14 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://careers.oracle.com/en/sites/jobsearch/job/333276/ - Excerpt: Data Center Integrated Planning & Scheduling Lead United States, US We are seeking a strategic and operationally strong leader to establish and scale integrated planning and scheduling standards across OCI's global data center delivery portfolio. Operating within the Chief of Staff organization, this role is responsible for developing enterprise-level scheduling governance, standardized planning frameworks, milestone structures, and portfolio-level schedule visibility that enable predictable, scalable delivery across rapidly expanding programs and campuses. This role will partner closely with Program E2E, PMO, Construction Delivery, Long Range Planning, Cost Controls, Design, TPM, and site scheduling teams to drive consistency in how projects are planned, baselined, tracked, escalated, and reported. Core Responsibilities Enterprise Planning & Schedule Governance Develop and maintain enterprise scheduling standards, planning frameworks, and governance processes across OCI construction programs Establish standardized milestone structures, critical path methodologies, schedule maturity expectations, and baseline governance practices Define enterprise expectations for: schedule development schedule updates change management forecasting recovery planning variance reporting Drive consistency in scheduling practices across regions, campuses, and delivery teams Integrated Program & Portfolio Planning Support development of integrated portfolio-level planning frameworks connecting: long range planning design procurement construction commissioning operational readiness Partner with Long Range Planning and Program E2E teams to support pipeline planning and scalable campus delivery sequencing Ensure enterprise-level visibility into major dependencies, sequencing risks, and delivery constraints across the portfolio Schedule Visibility & Executive Reporting Establish portfolio-level schedule health reporting, trend analysis, and milestone visibility frameworks Develop standardized executive reporting structures focused on: milestone attainment critical path risks ### Sales Strategy Senior Analyst, CRO Analytics - Salesforce - Location: Washington - Seattle; California - San Francisco (unspecified) - Salary: $119K-$164K - Posted: 2026-06-01 - Parental leave: 26 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://careers.salesforce.com/en/jobs/jr344168/sales-strategy-senior-analyst-cro-analytics/ - Excerpt: Sales Strategy Senior Analyst, CRO Analytics Washington - Seattle; California - San Francisco We're looking for a highly skilled Tableau expert to join our Global Sales Strategy team. In this critical role, you will be a key architect and developer for our new global standard reporting infrastructure for the entire Salesforce Sales organization. This is a unique opportunity to build gold-standard dashboards and inventive, intuitive analytics tools that will serve as the cornerstone for our sales and strategy teams. You will help lead the charge on this initiative, driving the global adoption of your reporting and setting the benchmark for "Tableau on Tableau" both internally and externally. What You'll Be Building... Gold-Standard Dashboards: Develop and deliver insightful dashboards that serve as the single source of truth for key metrics, including ACV, pipeline, NNAOV, and forecasting. Efficient Data Models: Build efficient and performant data models using tools like Snowflake, Tableau Prep, or Tableau Relationships to ensure a clean, reliable, and scalable foundation for all reporting. Data Stewardship: Act as a data steward, ensuring the integrity and timeliness of critical sales data. You will also work directly with our audience to address technical issues or implement feedback suggestions to continuously improve the reporting experience. Strategic Collaboration: Partner with cross-functional teams within Sales Operations and beyond to define consistent reporting standards and best practices. About You... Tableau Expert. You have extensive hands-on experience ( 3 + years) in building complex, performant, and user-friendly Tableau dashboards. You can visualize data in a way that ### Robotics Software Engineer - Intuitive Surgical, Inc. - Location: Sunnyvale, CA, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Parental leave: 8 weeks (not source-backed) - Non-birth-parent leave: 8 weeks (not source-backed) - Apply: https://jobs.smartrecruiters.com/Intuitive/744000127977199-robotics-software-engineer - Excerpt: Robotics Software Engineer Sunnyvale, CA, United States Company Description: Primary Function of the Position In this role, you will help develop a next-generation medical robotics platform. You'll collaborate within a small, fast-paced team to iteratively design and build complex robotic prototypes. The ideal candidate is a self-driven software engineer with strong problem-solving skills, deep expertise C++ and robotics algorithms. Essential Job Duties Quickly learn an existing software codebase to implement and adapt the software stack Collaborate cross-functionally with controls, mechanical, and software engineers to design, build, and iterate on exploratory prototypes Design and lead experiments to methodically characterize system performance, accuracy, and reliability, and to de-risk key aspects of a novel robotic platform Refine prototype software into robust, production-quality code Architect clean, modular, and testable software interfaces and system designs for a distributed robotic platform Contribute to the long-term software architecture and platform strategyDevelop and maintain formal design control documentation in compliance with medical device standards Develop and maintain formal design control documentation in compliance with medical device standards Job Description: Required Skills and Experience Deep expertise in C++, object-oriented programming, software architecture design, and testing Strong working knowledge of robotics algorithms, including forward kinematics Excellent communication skills High levels of independence and technical ownership Full-stack mentality, with flexibility to contribute to different areas of the codebase Required Education and Training MS or PhD in computer science, mechanical engineering, or equivalent Working Conditions None Preferred Skills and Experience Four years of experience developing software applications Familiarity with development in a ### Manager, Business & Project Management Office (BPMO) - AbbVie Inc. - Location: North Chicago, IL, United States (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013438684-manager-business-project-management-office-bpmo- - Excerpt: Manager, Business & Project Management Office (BPMO) North Chicago, IL, United States Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: The Manager, Business & Project Management Office (BPMO) plays a critical role within AbbVie's Business Technology Solutions Information Research (IR) Team, leading cross-functional delivery, process optimization, annual planning and supporting reporting, resource management and project management office activities within the BPMO team. This role is responsible for driving alignment across stakeholders to help support continuous improvement of processes, planning, tools and standards that strengthen IR's operational performance and value delivery. Responsibilities: Drive end-to-end delivery of cross-functional initiatives within IR, ensuring alignment to stakeholders, scope, timelines, budget, and quality expectations. Identify, design, and implement process improvements across BPMO and IR workflows, tools, and standards to enhance operational efficiency and consistency. Lead IR annual planning processes (e.g., Long-Range Plan, Capital Plan), ensuring initiatives and funding support IR strategic priorities. Provide accurate, timely reporting and insights to IR leadership, enabling data-driven decision-making and transparent communication. Effectively leverage established PPM practices and tools (e.g., Clarity, Jira). Support and partner with ### Senior Data Center Facilities Engineer I - Oracle - Location: Ashburn, VA, United States, US (unspecified) - Salary: $102K-$210K - Posted: 2026-06-11 - Parental leave: 14 weeks (not source-backed) - Non-birth-parent leave: 14 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://careers.oracle.com/en/sites/jobsearch/job/335887/ - Excerpt: Senior Data Center Facilities Engineer I Ashburn, VA, United States, US Tracks and monitors ongoing Data Center critical infrastructure maintenance and repair for all service lines to pre-defined service level agreements (SLAs). Manages incidents that impact Data Center infrastructure services and the proactive and timely resolution of such incidents. Conducts site reviews and assessments to evaluate suitability for data center builds. Acts as the engineering representative on a wide range of moderately complex on-site scenarios related to mission critical systems, operations, and functionality. Provides engineering insight to ensure project or other design initiatives align with company expectations. Contributes to the identification of training programs for newer members of the team, acting as a subject matter expert with many standard systems and trains others on the team. Key Responsibilities Critical Environment Maintenance Support: - Tracks and monitors ongoing critical environment maintenance and repair for all service lines to pre-defined service level agreements (SLAs) to ensure service uptime is maintained to the highest standards and that faults are dealt with promptly. -Employs practical operating knowledge of engineering systems to lead standard diagnostics and repairs, escalating blockers or obstacles when needed. -Applies knowledge of Oracle processes, procedures, and industry standards to resolve routine issues. -Offers suggestions for system-level enhancements to reduce potential problems. -Evaluates the suitability of components, processes, or action plans. Incident Management and Operation Improvement: - Manages incidents that impact data center infrastructure and the proactive and timely resolution of such incidents. -Collaborates with design, construction, commissioning, facility engineering, and data ### Senior Data Center Facilities Engineer - Oracle - Location: Thailand, TH (unspecified) - Salary: Not disclosed - Posted: 2026-06-05 - Parental leave: 14 weeks (not source-backed) - Non-birth-parent leave: 14 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://careers.oracle.com/en/sites/jobsearch/job/335883/ - Excerpt: Senior Data Center Facilities Engineer Thailand, TH Tracks and monitors ongoing Data Center critical infrastructure maintenance and repair for all service lines to pre-defined service level agreements (SLAs). Manages incidents that impact Data Center infrastructure services and the proactive and timely resolution of such incidents. Conducts site reviews and assessments to evaluate suitability for data center builds. Acts as the engineering representative on a wide range of moderately complex on-site scenarios related to mission critical systems, operations, and functionality. Provides engineering insight to ensure project or other design initiatives align with company expectations. Contributes to the identification of training programs for newer members of the team, acting as a subject matter expert with many standard systems and trains others on the team. Key Responsibilities Critical Environment Maintenance Support: - Tracks and monitors ongoing critical environment maintenance and repair for all service lines to pre-defined service level agreements (SLAs) to ensure service uptime is maintained to the highest standards and that faults are dealt with promptly. -Employs practical operating knowledge of engineering systems to lead standard diagnostics and repairs, escalating blockers or obstacles when needed. -Applies knowledge of Oracle processes, procedures, and industry standards to resolve routine issues. -Offers suggestions for system-level enhancements to reduce potential problems. -Evaluates the suitability of components, processes, or action plans. Incident Management and Operation Improvement: - Manages incidents that impact data center infrastructure and the proactive and timely resolution of such incidents. -Collaborates with design, construction, commissioning, facility engineering, and data center operations teams to ### Contracts Administrator 2-Fin - Oracle - Location: BENGALURU, KARNATAKA, India, IN (unspecified) - Salary: Not disclosed - Posted: 2026-06-09 - Parental leave: 14 weeks (not source-backed) - Non-birth-parent leave: 14 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://careers.oracle.com/en/sites/jobsearch/job/325584/ - Excerpt: Contracts Administrator 2-Fin BENGALURU, KARNATAKA, India, IN The Lead Specialist - Customer Deal Desk is responsible for drafting, reviewing, and managing contractual documents to support Sales-led deal execution. This is a non-customer-facing role that works behind the scenes to enable Sales and Legal teams. The role focuses on preparing and redlining contracts for negotiation and ensuring contract readiness for execution. The position works closely with internal stakeholders including Sales, Legal, Finance, and Operations to ensure contracts are accurate, compliant, and processed within defined timelines. Success in this role requires strong attention to detail, solid understanding of commercial terms, and the ability to operate effectively in a high-pressure, high-volume environment. Key Responsibilities Draft, review, and prepare contract documents and redlines (sales agreements, amendments, NDAs, vendor contracts) in alignment with company policies and standard templates Support the contract lifecycle from request intake through drafting, validation, and submission for approvals Prepare and redline contracts to support negotiation; ensure contract readiness for execution Partner with Sales and internal stakeholders to ensure contract completeness, accuracy, and alignment with commercial terms Ensure adherence to standard templates, playbooks, and compliance requirements Identify and flag risks, inconsistencies, or deviations from standard terms; escalate to appropriate stakeholders as needed Maintain accurate and complete documentation within internal systems (e.g., Q system) for auditability and tracking Track contract progress and ensure timely turnaround in line with defined SLAs/TATs, especially during peak business cycles Collaborate with cross-functional teams to address process gaps and improve turnaround efficiency Contribute to process improvements, standardization, and ### Project Engineer (fixed-term contract) - AbbVie Inc. - Location: Campoverde, Lazio, Italy (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013509096-project-engineer-fixed-term-contract- - Excerpt: Project Engineer (fixed-term contract) Campoverde, Lazio, Italy Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Per il sito di Campoverde, siamo alla ricerca di una risorsa per un contratto a tempo determinato/temporary assignment per il ruolo di Project Engineer con le seguenti responsabilità: Gestione di progetti comportanti investimenti di capitale dalla fase della proposta di budget passando per lo studio di fattibilità, la stima dei costi e dei tempi, la redazione dell'eventuale giustificazione economica. Sviluppo del progetto con definizione degli user requirement coinvolgendo tutti gli enti interni interessati,(utilizzatore finale, EHS, Q.A., Manutenzione,etc.), inglobando le norme di buona fabbricazione, le norme di buona tecnica, gli Abbott Engineering Standards & Specifications e gli Abbott Technical Standard in materia EHS. La scelta degli equipment, facilities e delle forniture in genere deve soddisfare le esigenze di progetto. Realizzazione degli impianti, dei locali e delle facilities necessarie alla funzionalità del progetto con la responsabilità dei tempi e degli esborsi. Organizzazione dei collaudi di sicurezza, funzionali e prestazionali, le Pre-Start-Up Safety Review,gli start-up e le sezioni di training per il personale. Fornire ### Head of Integrated Planning - Corning - Location: Charlotte, NC (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://corningjobs.corning.com/job/Charlotte-Head-of-Integrated-Planning-NC-28216/1373535800/ - Excerpt: Head of Integrated Planning Charlotte, NC Requisition Number: 73961 The company built on breakthroughs. ​ Join us.​ Corning is one of the world's leading innovators in glass, ceramic, and materials science. From the depths of the ocean to the farthest reaches of space, our technologies push the boundaries of what's possible. ​ How do we do this? With our people. They break through limitations and expectations - not once in a career, but every day. They help move our company, and the world, forward. ​ ​At Corning, there are endless possibilities for making an impact. You can help connect the unconnected, drive the future of automobiles, transform at-home entertainment, and ensure the delivery of lifesaving medicines. And so much more.​ ​Come break through with us. The Global Supply Management (GSM) Function is recognized as a critical function for business success. It delivers the training, tools and opportunities needed to create innovative solutions for the function & the corporation. GSM has leading edge, effective processes to anticipate and exceed customer requirements. Role Scope: Corning Inc. is seeking a senior Supply Chain leader to join the Integrated Planning transformation team. As a key player in our Supply Chain transformation, this role will focus on building the global supply chain planning capabilities and standards for Corning, as well as partnering with Corning's businesses to lead their planning transformation journey towards best-in-class practices. This leader will oversee the design, development ### Senior Manager, Data Center Operations - Oracle - Location: West Jordan, UT, United States, US (unspecified) - Salary: $126K-$264K - Posted: 2026-06-09 - Parental leave: 14 weeks (not source-backed) - Non-birth-parent leave: 14 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://careers.oracle.com/en/sites/jobsearch/job/336362/ - Excerpt: Senior Manager, Data Center Operations West Jordan, UT, United States, US Oversees Data Center Operations across multiple data centers, managing and integrating team performance, operations metrics, and capacity analysis into the broader business line strategy. Directs multiple teams in supporting escalated technical issues, crisis management, and root cause analysis, while standardizing processes and maintaining an accurate knowledge base. Leads new region builds and expansion activities, acting as a senior liaison with project and engineering teams to manage timelines, capacity, and ensure adherence to world-class standards. Guides teams responsible for installations, repairs, inventory, and logistics, enforces standards for component replacements and upgrades, recommends significant purchases, and implements advanced maintenance strategies to optimize data center efficiency and stability. Key Responsibilities Data Center Site Portfolio Management: - Oversees Data Center Operations team across multiple data centers. Performance Monitoring and Analysis: -Oversees multiple teams, integrates operations metrics into broader business line strategy. -Directs performance evaluations for multiple teams, integrates findings into broader business line strategy. -Supervises analysis of physical, power, and cooling capacity for multiple teams, integrates findings into broader business line strategy. -Leads Guides collaboration across functions to support continuous improvement efforts in alignment with industry best practices, and mentors team members. Issue Management and Automation: -Directs multiple teams providing support for escalated complex technical issues. -Proposes and implements advanced strategies for issue triage and leverages automation, scheduling, and monitoring tools to prevent and resolve potential problems. -Identifies, documents, and standardizes issues, processes, and solutions, ensuring consistency and accuracy in the data center ### Safety Manager - Bunge - Location: Amsterdam (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Parental leave: 6 weeks (not source-backed) - Non-birth-parent leave: 6 weeks (not source-backed) - Apply: https://jobs.bunge.com/job/Amsterdam-Safety-Manager-1013-BK/1384598333/ - Excerpt: Safety Manager Amsterdam Requisition Number: 45024 Are you a seasoned safety leader with a passion for creating a truly safe, healthy, and future-proof work ? At Bunge, we believe that safety is paramount. As our new Safety Manager at the Bunge plant in Amsterdam, you will play a critical role in ensuring the highest standards of health, safety, and excellence across all our people, processes, and operations. This vital leadership role places you at the heart of our commitment to safety. You will be responsible for planning, organizing, supervising, managing, and continuously improving the full spectrum of Bunge Global's safety, occupational health, and standards, policies, and procedures. Your strategic mindset and strong on-the-floor presence will directly contribute to preventing incidents, safeguarding our people and facilities, and embedding a mature, proactive safety culture across our site. Your Impact at Bunge: In this dynamic senior role, you will champion a safety‑first mindset, lead the site's safety function, and drive continuous improvement. Key responsibilities include: Safety Leadership & Strategic Implementation: As the primary safety leader on site, you shape the safety strategy and translate Bunge's Global standards into actionable, high-impact initiatives. You will oversee the performance of safety KPIs, ensure alignment with the Plant Manager and regional Health and Safety organization, and guarantee the effectiveness of safety systems, compliance programs, audits, and critical sa ### Chief Compliance Officer (CCO) for Truist Investment Services, Inc. and Truist Advisory Services, Inc. - Truist Financial Corporation - Location: 3 Locations (unspecified) - Salary: Not disclosed - Posted: 2026-05-29 - Parental leave: 10 weeks (not source-backed) - Non-birth-parent leave: 10 weeks (not source-backed) - Apply: https://truist.wd1.myworkdayjobs.com/Careers/job/Charlotte-NC/Chief-Compliance-Officer--CCO--for-Truist-Investment-Services--Inc-and-Truist-Advisory-Services--Inc_R0113564 - Excerpt: Chief Compliance Officer (CCO) for Truist Investment Services, Inc. and Truist Advisory Services, Inc. 3 Locations posted: Posted 14 Days Ago ### Sr. Quality Engineer - Corning - Location: Tucheng City (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://corningjobs.corning.com/job/TuCheng-City-Sr_-Quality-Engineer-236/1384425900/ - Excerpt: Sr. Quality Engineer Tucheng City Role Purpose Handles quality-related issues and abnormalities by identifying root causes, implementing corrective actions, and driving preventive measures to ensure long-term resolution and continuous improvement. Supports the understanding and implementation of the Quality Management System and Product Quality Architecture, ensuring compliance with internal and external specifications and standards. Key Responsibilities Assists in applying and maintaining quality evaluation and control systems for processing materials into finished or partially finished products. Collaborates with engineering and manufacturing teams to uphold quality standards throughout production processes. Contributes to inspecting, testing, and evaluating products and production equipment under established methods and procedures. Conduct quality assurance tests and performs statistical analysis to identify non-conforming products or materials. Participates in auditing quality systems to identify deficiencies and supports corrective actions and improvement efforts. Learns and applies basic concepts of product design, incoming material inspection, production control, product evaluation, and reliability testing under guidance. Provides assistance to team members and managers on smaller projects, supporting the use of quality tools and methods to achieve team goals. Follows standard practices and procedures to analyze situations or data and assists in identifying solutions under supervision. Experiences/Educ ### Data Center Site lead - Oracle - Location: Malaysia, MY (unspecified) - Salary: Not disclosed - Posted: 2026-06-05 - Parental leave: 14 weeks (not source-backed) - Non-birth-parent leave: 14 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://careers.oracle.com/en/sites/jobsearch/job/335840/ - Excerpt: Data Center Site lead Malaysia, MY As the Data Center Site Lead, you will play a crucial role in maintaining the availability and security of our data center. Your responsibilities will involve close collaboration with colocation providers and key stakeholders to ensure 100% data center uptime. You will work hand-in-hand with access management and security systems to adhere to Oracle's stringent data center security standards. Additionally, you will actively manage incident, change, and problem management for data center space, cooling, and power systems. Your proactive approach to identifying and mitigating risks associated with data center operations will be vital to the success of this role. Collaborate with colocation providers and stakeholders to maintain 100% data center availability. Ensure adherence to Oracle's data center security standards through close coordination with access management and security systems. Manage incident, change, and problem management for data center space, cooling, and power systems. Proactively identify and mitigate risks associated with data center operations. Initiate corrective and preventive actions on incidents and implement global best practices. Develop and maintain strong relationships with internal teams and external partners. Stay updated on industry trends and best practices in data center management. Provide regular reports and updates on data center performance and security. Oversee and mentor a team of data center technicians and engineers. Ensure compliance with all relevant regulations and standards. Career Level - IC4 ### EHS Engineer - Corning - Location: Tucheng City (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://corningjobs.corning.com/job/TuCheng-City-EHS-Engineer-236/1380382000/ - Excerpt: EHS Engineer Tucheng City Role Purpose This role ensures compliance with occupational safety, health, and environmental regulations by implementing clearly defined EHS practices aligned with Corning global standards. The EHS Engineer supports risk identification, regulatory execution, and continuous improvement to maintain safe and compliant factory operations and sustainable. Key Responsibilities Execute monthly environmental regulatory reporting by collecting required data, completing standard forms, and submitting reports according to government timelines. Perform routine EHS risk assessments by identifying hazards, participating in risk rating, and documenting findings. Support EHS improvement actions by tracking corrective and preventive actions and following up implementation progress. Update internal procedures in response to new or revised regulations based on defined legal registers and guidance. Deploy Corning EHS policies by translating requirements into site-level practices and coordinating related activities. Deliver EHS training sessions and provide on-site consultation based on established materials and standards. Experiences/Education - Required Bachelor's degree or above in Occupational Safety, Industrial Safety, Environmental Health, or similar disciplines. Basic knowledge of Taiwan EHS regulations, including ability to identify applicable laws, understand compliance requirements, and execute tasks under established procedures. Basic EHS risk assessment capability, including hazard i ### Senior Executive - Packaging - Bunge - Location: Kandla (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Parental leave: 6 weeks (not source-backed) - Non-birth-parent leave: 6 weeks (not source-backed) - Apply: https://jobs.bunge.com/job/Kandla-Senior-Executive-Packaging-GJ-370140/1400343933/ - Excerpt: Senior Executive - Packaging Kandla Requisition Number: 45928 Business Title: Senior Executive - Packaging Reporting to: Senior Manager - Packaging Role Purpose Statement: • Ensuring for Packing of Vanaspati & edible oils with Standard parameters as designed by Bunge Main Accountabilities: • Packaging of Edible oil under the well knows brand names. • Adhering to Safety & food Standards and goals and implementing stringent manufacturing practices conforming to HACCP standards. • Developing cost effective manufacturing solutions to reduce overall packing cost. Continuous improvement in packing materials & procurers. • Training of packaging team - Functional identification of training needs (Both Technical & Behavioral) for the packing team. Also to practice TQM/5S,CI, KAIZEN, food safety etc.. and ensure continuous improvements at work by involving all department / division members in small group activities / problem solving exercises. • Ensure Packing is executed with required Quality and as per Food safety norms. • Accountable for Inventory Control of all Raw Materials, Packing Materials, Finished Goods, Spares & Tools. • Responsible for Identification, analysis and simplification / Improvements of processes in operations. • Responsible for keeping operation area safe for workmen. • Responsible for delivering rated capacity output per shift. • Sustain the 5s & housekeeping in plant. • Minimize the waste in respect to oil and packing materials. • To attend and arrest Market complaints. Knowledge and Skills: • Kn ### Quality and Food Safety Manager/Coordinator - Bunge - Location: Kruszwica (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Parental leave: 6 weeks (not source-backed) - Non-birth-parent leave: 6 weeks (not source-backed) - Apply: https://jobs.bunge.com/job/Kruszwica-Quality-and-Food-Safety-ManagerCoordinator-Kuya-88-150/1378290633/ - Excerpt: Quality and Food Safety Manager/Coordinator Kruszwica Requisition Number: 44242 Responsibilities: System Management: Develop, implement, and maintain comprehensive Food Safety and Quality Assurance (FSQA) programs, including HACCP, GMP, SOPs, and other relevant quality systems (e.g., BRC, IFS, GFSI standards) to ensure compliance with regulatory and customer requirements. Compliance & Auditing: Oversee and manage internal and external audits, including those from regulatory bodies, third-party certification bodies, and customers. Drive corrective and preventive actions resulting from audit findings to ensure continuous improvement. Quality Control: Manage the quality control of raw materials, in-process production, and finished products, ensuring adherence to established specifications and standards. Team Leadership & Training: Lead, mentor, and provide ongoing training and support to the QFS team and production personnel on food safety protocols, quality standards, and compliance procedures. Foster a strong food safety culture across all departments. Regulatory Adherence: Stay current with all applicable local, national, and international food safety regulations and industry best practices, translating these into updated internal policies and procedures. Issue Resolution: Investigate and resolve quality and food safety issues, including customer complaints, non-conformances, and product recalls, by conducting root cause analyses and implementing effective solutions. Continuous Improvement: Analyze quality data, identify trends, ### Contract Manufacturer Manager (Teradyne, Penang) - Teradyne - Location: Penang (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Parental leave: 4 weeks (not source-backed) - Non-birth-parent leave: 4 weeks (not source-backed) - Apply: https://jobs.teradyne.com/Teradyne/job/PENANG-Contract-Manufacturer-Manager-%28Teradyne%2C-Penang%29/1344719200/ - Excerpt: Contract Manufacturer Manager (Teradyne, Penang) Penang Our Purpose TERADYNE, where experience meets innovation and driving excellence in every connection. We are fueled by creativity and diversity of thought and in our workforce. Our employees are supported to innovate and learn something new every day. We cultivate a culture of inclusion for all employees that respects their individual strengths, views, and experiences. We believe that our differences enable us to be a better team - one that makes better decisions, drives innovation and delivers better business results. Opportunity Overview The Contract Manufacturing Manager is responsible for leading and managing Teradyne's contract manufacturing operations across multiple sites and sources. This role ensures standardized KPI metrics, drives operational excellence, and achieves company goals for On-Time Delivery (OTD), quality, and cost efficiency. The manager will foster strong partnerships with contract manufacturers, implement continuous improvement initiatives, and maintain alignment with Teradyne's strategic objectives. Operational Leadership Oversee contract manufacturing operations base in major contract manufacturing partner site. Ensure alignment with Teradyne's standards for capacity, OTD, quality, and cost. Performance Management Define, implement, and monitor standardized KPI metrics in contract manufacturers. Drive accountability for meeting performance targets and escalate issues proactively. Continuous Improvement Lead initiatives to improve efficiency, reduce wa ### Principal Controls Engineer- Data Center Design and Innovation - Oracle - Location: United States, US (unspecified) - Salary: $146K-$306K - Posted: 2026-06-11 - Parental leave: 14 weeks (not source-backed) - Non-birth-parent leave: 14 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://careers.oracle.com/en/sites/jobsearch/job/336862/ - Excerpt: Principal Controls Engineer- Data Center Design and Innovation United States, US This is a highly influential technical leadership role focused on defining the future of Building Management Systems (BMS) and Electrical/Mechanical Plant Management Systems (EMPS) for OCI's hyperscale and GW-scale data center platforms. You will provide deep technical expertise in controls architecture, software integration, automation, operational intelligence, and platform standardization to enable world-class reliability, scalability, efficiency, and speed of deployment. You will partner closely with mechanical, electrical, network, software, operations, commissioning, manufacturing, and supply chain engineering teams to develop and scale a unified controls ecosystem supporting OCI's next-generation infrastructure. This role is ideal for a hands-on technical leader who enjoys solving complex engineering challenges, influencing strategy through expertise, and driving innovation without direct people management responsibilities. What You'll Do Technical Strategy & Architecture Define and evolve the technical architecture for BMS and EMPS controls systems across OCI's global data center portfolio. Develop long-term controls and automation roadmaps supporting hyperscale cloud and AI infrastructure growth. Establish standardized controls philosophies, software frameworks, integration architectures, and deployment models. Drive innovation in software-driven infrastructure management focused on resiliency, automation, telemetry, observability, and operational efficiency. Provide technical leadership for controls integration across mechanical, electrical, thermal, and critical infrastructure systems. Standards & Engineering Excellence Develop global engineering standards, design guidelines, software requirements, and integration protocols for BMS/EMPS platforms. Define controls cybersecurity, alarming, telemetry, redundancy, and data integrity requirements for mission-critical operations. Create scalable design patterns that ensure consistency across regions, vendors, and deployment models. Establish validation, ### Oracle Health - Oncology Clinical Consultant - Oracle - Location: United States, US (unspecified) - Salary: $82K-$166K - Posted: 2026-06-08 - Parental leave: 14 weeks (not source-backed) - Non-birth-parent leave: 14 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://careers.oracle.com/en/sites/jobsearch/job/333771/ - Excerpt: Oracle Health - Oncology Clinical Consultant United States, US The Oncology Clinical Venue Strategist, working collaboratively with Solution Strategists, VA Solution Experts, and National Council Tier 1 Subject Matter Experts (SMEs), bridges clinical insight with technical execution-guiding teams to deliver consistent, standardized, and mission-aligned workflows that enhance care delivery across the federal enterprise. The Clinical Venue Strategist serves as the principal clinical advisor for a designated service line(s) or solution(s) within the Federal Electronic Health Record Modernization (FEHRM) initiative, blending deep clinical expertise with advanced knowledge of Oracle Cerner Millennium solutions to drive seamless integration, optimize workflows, and elevate clinical performance across Federal healthcare systems. By staying current with national design standards, regulatory requirements, and clinical best practices, Clinical Venue Strategist guide implementation teams, facilitate cross-venue collaboration, and lead national-level testing and workflow standardization efforts. Ultimately, this role is critical to FEHRM's mission of delivering a unified, interoperable electronic health record across Federal agencies, transforming healthcare delivery for service members, Veterans, and their families.The Clinical Venue Strategist, working collaboratively with Solution Strategists, VA SEs, and National Council Tier 1 Subject Matter Experts (SMEs), bridges clinical insight with technical execution-guiding teams to deliver consistent, standardized, and mission-aligned workflows that enhance care delivery across the federal enterprise. The Clinical Venue Strategist serves as the principal clinical advisor for a designated service line(s) or solution(s) within the Federal Electronic Health Record Modernization (FEHRM) initiative, blending deep clinical expertise with advanced knowledge of Oracle Cerner Millennium solutions to drive seamless integration, optimize workflows, and ### Specialist, Manufacturing QA - AbbVie Inc. - Location: Sligo, SO, Ireland (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013245756-specialist-manufacturing-qa - Excerpt: Specialist, Manufacturing QA Sligo, SO, Ireland Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: In AbbVie Ballytivnan, we are recruiting for a QA Manufacturing Compliance Specialist to join our team. This position will report into the Quality Operations Lead and support the Quality Assurance team. The QA Manufacturing Specialist is responsible for documenting and establishing a quality system which ensures full compliance with all regulatory and AbbVie requirements. The QA Manufacturing Compliance Specialist will have responsibility to assess and report on the effectiveness of the quality system to senior management. This role requires shift work. What you will do: Ensure that all products leaving AbbVie Biologics Ballytivnan meet the standards required for marketed and investigational drug products. Ensure that products and aseptic process simulations manufactured at AbbVie Biologics Ballytivnan meet the requirements of the end users, regulatory authorities and of the company. Provide quality and compliance oversight and assistance to the Operations function of the company to manufacture products in compliance with all site policies and procedures. Provide quality oversight during the aseptic processing of products, ### QA Operations Compliance Specialist - AbbVie Inc. - Location: Sligo, SO, Ireland (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013594016-qa-operations-compliance-specialist - Excerpt: QA Operations Compliance Specialist Sligo, SO, Ireland Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Innovate with intention. Science is at the heart of what we do. People are at the heart of why we do it. Welcome to AbbVie! We are a global, research-based biopharmaceutical company that combines the focus and passion of leading-edge biotech with the expertise and capability of an established pharmaceutical leader. Redefining what is possible is our business and our passion. Our goal is to help patients live healthier lives and we are proud to be a Great Place to Work. We are recruiting a QA Operations Compliance Specialist to join our site in Ballytivnan, Sligo. Are you intrigued? Do you want to learn more? A snapshot of your key responsibilities as a QA Operations Compliance Specialist would be: Ensuring that all products leaving AbbVie Biologics department meet the standards required for marketed and investigational drug products. Ensuring that products and aseptic process simulations manufactured at AbbVie Biologics meet the requirements of the end users, regulatory authorities and of the company. ### Warehouse Associate - Bunge - Location: Sandston, VA (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Parental leave: 6 weeks (not source-backed) - Non-birth-parent leave: 6 weeks (not source-backed) - Apply: https://jobs.bunge.com/job/Sandston-Warehouse-Associate-VA-23150/1383271033/ - Excerpt: Warehouse Associate Sandston, VA Requisition Number: 44657 A Day in the Life: Warehouse Associates are the last company personnel to handle finished product prior to customer delivery; therefore, operators need to have clear understanding of product packaging standards and transportation equipment standards. Knowledge of product descriptions, palletizing methods, and lot numbers is required to ensure accurate order processing. Proper loading ensures that trailer weights meet state and interstate highway weight requirements, and that our product arrives at the customer free of damage. Candidate must actively participate in Bunge's Employee Safety Policy and maintain a safe work environment for self and all employees. Position Details: Work Schedule: Monday through Friday, 8-hour shifts: 1st Shift: (6:30a-3:00p), 2nd Shift: (2:30p-11:00p), 3rd Shift: (10:30p-7:00a) with occasional overtime as needed. Starting pay is $16.50 per hour. This role is eligible to receive an annual incentive bonus. What You'll Be Doing: Work consistently in a safe manner. Perform basic order selection, picking, palletizing, and loading functions for finished product orders, which includes the following: Inspect trailers to be loaded to ensure company standards are met. Decide proper load stacking and sequence following FIFO.Verify product codes, lot numbers, and item counts. Prepare correct picking and loading records to facilitate accurate transportation documents and customer receiving documents. This will ensure accurate accountin ### Compliance & Obligation Manager (f/m/d) - SAP - Location: Region Europe | Country Germany | Internal Posting Location Walldorf (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Parental leave: 6 weeks (not source-backed) - Non-birth-parent leave: 6 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.sap.com/job/Walldorf-Compliance-&-Obligation-Manager-%28fmd%29-69190/1398453333/ - Excerpt: Compliance & Obligation Manager (f/m/d) Region Europe | Country Germany | Internal Posting Location Walldorf We help the world run better At SAP, we keep it simple: you bring your best to us, and we'll bring out the best in you. We're builders touching over 20 industries and 80% of global commerce, and we need your unique talents to help shape what's next. The work is challenging - but it matters. You'll find a place where you can be yourself, prioritize your wellbeing, and truly belong. What's in it for you? Constant learning, skill growth, great benefits, and a team that wants you to grow and succeed. What you'll build Continues improve, develop, implement, and manage the Information Security Management Systems including IT Grundschutz building blocks and scope extension in line with BSI standards and methodologies. Establish and support strategies and initiatives to comply with Information Security Compliance standards and address emerging threats. Support internal audits and compliance assessments, preparing reports and documentation for internal & external assessments, checks, and audits. Provide expert guidance and mentorship to various teams & stakeholders, promoting knowledge-sharing and skills growth from IT Grundschutz and Information Security best practices. Conduct and orchestrate comprehensive risk assessments and develop response strategies to protect cloud-based IT-systems and supporting processes. Collaborate with internal stakeholders and external partners to ensure seamless implementation of information security standards. Establish and manage compliance policies a ### Senior Clinical Consultant - Oracle - Location: United States, US (unspecified) - Salary: $31.83-$63.65/hr - Posted: 2026-06-01 - Parental leave: 14 weeks (not source-backed) - Non-birth-parent leave: 14 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://careers.oracle.com/en/sites/jobsearch/job/335381/ - Excerpt: Senior Clinical Consultant United States, US Responsible for driving the client through the design of clinical and business processes, solution and technology workflow, and successful adoption that will lead to achieved value. Manage ongoing relationships with clients, providing account management and clinical subject matter expertise focusing on client success in utilizing Oracle's solutions. Through the use of Oracle's implementation approach and methodology, the Consultant will assist in change management, help identify opportunities for improvement, and is accountable for achieving the project's targeted outcomes. Entry-level position that acts as a liaison between the clinical and IT departments, leveraging clinical knowledge specific to a domain expertise (Healthcare, informatics, clinical) to provide innovative solutions. Responsible for applying statistical, research, clinical theories and methods to solve problems. As a member of the team, follows standard practices and procedures to evaluate and analyze data, develop analysis and studies and provide new product offering and innovations to external customer engagements. Work involves using analytical skills sufficient to interpret data/ instructions with assistance and guidance in understanding and applying the relevant customer standards with limited autonomy. Receives general instruction on routine work and detailed instruction on new projects or assignments. Must have knowledge in reference to regulations and standard operating procedures. Maintains a high level of professional expertise through familiarity with domain literature and reports. Strong understanding of healthcare strategy, operations, and ability to adjust to changing industry regulatory requirement Disclaimer: Certain U.S. based or U.S. customer or client-facing roles may be required to comply with applicable ### Trade Compliance Analyst - Intuitive Surgical, Inc. - Location: Mexicali, MEXICO, Mexico (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Parental leave: 8 weeks (not source-backed) - Non-birth-parent leave: 8 weeks (not source-backed) - Apply: https://jobs.smartrecruiters.com/Intuitive/744000128261899-trade-compliance-analyst - Excerpt: Trade Compliance Analyst Mexicali, MEXICO, Mexico Company Description: It started with a simple idea: what if surgery could be less invasive and recovery less painful? Nearly 30 years later, that question still fuels everything we do at Intuitive . As a global leader in robotic-assisted surgery and minimally invasive care , our technologies-like the da Vinci surgical system and Ion -have transformed how care is delivered for millions of patients worldwide. We're a team of engineers, clinicians, and innovators united by one purpose: to make surgery smarter, safer, and more human. Every day, our work helps care teams perform with greater precision and patients recover faster, improving outcomes around the world. The problems we solve demand creativity, rigor, and collaboration. The work is challenging, but deeply meaningful-because every improvement we make has the potential to change a life. If you're ready to contribute to something bigger than yourself and help transform the future of healthcare , you'll find your purpose here. Job Description: Primary Function of Position: Under general supervision from the Senior Manager MX Trade Compliance, the Trade Compliance Analyst becomes responsible for applying trade compliance practices and policies within the business, identifying areas where they are out of compliance, and offering suggestions for how to make necessary modifications. This requires regular review and research into governing authorities' current rules and regulations. including but not limited to data collection, data analysis, continuous improvement, processes efficiency, process planning standardization, projects development, and automation among others all Trade Compliance operation's related ### Aseptic Operations Specialist - AbbVie Inc. - Location: Sligo, SO, Ireland (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013111104-aseptic-operations-specialist - Excerpt: Aseptic Operations Specialist Sligo, SO, Ireland Company Description: AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on X , Facebook , Instagram , YouTube , LinkedIn and Tik Tok . Job Description: At AbbVie, we are committed to delivering innovative medicines and solutions that make a remarkable impact on people's lives. Our employees are driven by a shared purpose, a culture of integrity and inclusion, and a focus on excellence in science, manufacturing, and patient care. At our Ballytivnan site in Sligo, we are seeking an experienced Aseptic Operations Specialist to join our team and support the continued delivery of safe, compliant, and high-quality aseptic manufacturing operations. The Role As an Aseptic Operations Specialist, you will act as a site subject matter expert for aseptic manufacturing and sterility assurance. You will provide technical and operational support across aseptic processes, partner closely with cross-functional teams, and help ensure that manufacturing activities are carried out in line with regulatory requirements, site procedures, and AbbVie standards. This role plays a key part in maintaining a strong culture of quality, compliance, continuous improvement, and speak-up behavior across the site. Key Responsibilities Act as ### Quality Assurance Manager - Medical Devices - AbbVie Inc. - Location: Sligo, SO, Ireland (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012313546-quality-assurance-manager-medical-devices - Excerpt: Quality Assurance Manager - Medical Devices Sligo, SO, Ireland Company Description: AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on X , Facebook , Instagram , YouTube , LinkedIn and Tik Tok . Job Description: AbbVie invites you to join our cutting-edge pharmaceutical facility in Sligo, nestled in a region known for its vibrant community and scenic beauty. Embrace an opportunity to grow your career while contributing to meaningful innovations that enhance global health. An exciting role has opened up on our Ballytivnan site in Sligo. We are currently looking for a Quality Manager overseeing the Medical Device Quality team, reporting to the Quality Site Head. You will oversee the whole quality function for the medical device business on site. You'll ensure compliance with quality standards and regulatory requirements, leading a dedicated team of quality professionals. Responsibilities Quality Assurance & Control: Oversee testing of raw materials, manufacturing quality control, and product validation. Team Leadership: Manage and lead a team responsible for compliance and quality oversight. Regulatory Compliance: Ensure adherence to corporate and regulatory requirements. Performance Reporting: Report on the performance of the quality management system to senior management. Issue ### Final Signatory - AbbVie Inc. - Location: Marlow, ENGLAND, United Kingdom (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013246756-final-signatory - Excerpt: Final Signatory Marlow, ENGLAND, United Kingdom Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Provide brand support for the preparation and final signatory approval of promotional and non-promotional material and activities Attend Brand Team Meetings to ensure Review agenda/focuses are communicated and understood Support the continued implementation of a Code Compliant system for all promotional and non-promotional activities throughout AbbVie and the marketplace, ensuring the company is in line with the Association of British Pharmaceutical Industry (ABPI) standards, the MHRA blue guide for advertising and promotion and all applicable international Codes of Practice (EFPIA, IFPMA, and respective National Codes and National Regulatory Bodies) at all times. Provision of workable compliant solutions to support business development opportunities/product launches and contribute to the development of marketing campaigns Independent, timely, accurate review and approval of materials in accordance with the relevant Codes of Practice. Make appropriate evaluations when undertaking material reviews, taking into account the risk profile in decision making Provide Guidance on UK code requirements to overseas affiliates and UK Affiliate as and when required Actively participate in ### Maintenance Technician (Fitter) – Nights - AbbVie Inc. - Location: Westport, MO, Ireland (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013312406-maintenance-technician-fitter-nights - Excerpt: Maintenance Technician (Fitter) – Nights Westport, MO, Ireland Company Description: AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on X , Facebook , Instagram , YouTube , LinkedIn and Tik Tok . Job Description: About the Role We are seeking a skilled Maintenance Technician (Fitter) - Nights to join our Maintenance Team. In this role you will play a key role in supporting the reliability, performance, and compliance of our manufacturing equipment and mechanical services. The shift pattern will be Monday - Friday Nights, but flexibility around shifts is important in this role. This role is focused on maintaining equipment uptime, supporting health and safety standards, ensuring quality and compliance, and helping drive continuous improvement across the business unit. You will work in a highly regulated environment where teamwork, technical expertise, and a proactive approach are essential. Key Responsibilities Perform planned and unplanned maintenance on mechanical services, plant, and equipment Diagnose equipment issues, identify root causes, and implement effective solutions Support improvements in machine and equipment effectiveness Source and identify required spare parts for equipment and systems Assist specialist vendors during preventative maintenance activities Participate in FATs, commissioning, and ### Senior Material handler - Intuitive Surgical, Inc. - Location: Parvomay, BULGARIA, Bulgaria (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Parental leave: 8 weeks (not source-backed) - Non-birth-parent leave: 8 weeks (not source-backed) - Apply: https://jobs.smartrecruiters.com/Intuitive/744000129724350-senior-material-handler - Excerpt: Senior Material handler Parvomay, BULGARIA, Bulgaria Company Description: It started with a simple idea: what if surgery could be less invasive and recovery less painful? Nearly 30 years later, that question still fuels everything we do at Intuitive . As a global leader in robotic-assisted surgery and minimally invasive care , our technologies-like the da Vinci surgical system and Ion -have transformed how care is delivered for millions of patients worldwide. We're a team of engineers, clinicians, and innovators united by one purpose: to make surgery smarter, safer, and more human. Every day, our work helps care teams perform with greater precision and patients recover faster, improving outcomes around the world. The problems we solve demand creativity, rigor, and collaboration. The work is challenging, but deeply meaningful- because every improvement we make has the potential to change a life. If you're ready to contribute to something bigger than yourself and help transform the future of healthcare , you'll find your purpose here. Job Description: Primary Function of Position: Proper storage and removal, including the transport of goods and materials, as well as ensuring the supply of production materials, auxiliary materials, and operating materials. Roles and Responsibilities: Execution of complex SAP transactions Masters all standard processes associated with the warehouse and supports other team members with problems Training of team members and trainees Support in the creation of new Kanban cycles in cooperation with production planning Is able to create and present presentations Independent processing of small projects in compliance with ### Manager, Manufacturing (Biologics Operations) - AbbVie Inc. - Location: Singapore, , Singapore (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013552306-manager-manufacturing-biologics-operations- - Excerpt: Manager, Manufacturing (Biologics Operations) Singapore, , Singapore Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Purpose: Provide leadership, support, and management of the manufacturing shifts and functions within Biologics Manufacturing in the areas of resource planning and management, workflow and training, decision making, cost management and employee/business development initiatives. Build and maintain strong collaborative inter and cross functional relationships to meet manufacturing deliverables in the areas of production, quality, safety, and financial demands of the function. Major Responsibilities: Provide direction and resource planning for existing production and new product introduction to meet manufacturing deliverables Ensures manufacturing deliverables in the areas of resource, materials, equipment and process performance are met Equip team with a positive and safe work environment to ensure manufactured product complies with quality and safety standards Develop and manage personnel through hiring, managing performance, and talent development Coach the team for growth by being the role model. Drive confidence through changes and various priorities Leads and influences cross functionally to seek the best outcomes for Bio Manufacturing Develop, manage, and control department operational expenses ### FPA Analyst - Intuitive Surgical, Inc. - Location: Mexicali, MEXICO, Mexico (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Parental leave: 8 weeks (not source-backed) - Non-birth-parent leave: 8 weeks (not source-backed) - Apply: https://jobs.smartrecruiters.com/Intuitive/744000129624392-fpa-analyst - Excerpt: FPA Analyst Mexicali, MEXICO, Mexico Company Description: It started with a simple idea: what if surgery could be less invasive and recovery less painful? Nearly 30 years later, that question still fuels everything we do at Intuitive . As a global leader in robotic-assisted surgery and minimally invasive care , our technologies-like the da Vinci surgical system and Ion -have transformed how care is delivered for millions of patients worldwide. We're a team of engineers, clinicians, and innovators united by one purpose: to make surgery smarter, safer, and more human. Every day, our work helps care teams perform with greater precision and patients recover faster, improving outcomes around the world. The problems we solve demand creativity, rigor, and collaboration. The work is challenging, but deeply meaningful-because every improvement we make has the potential to change a life. If you're ready to contribute to something bigger than yourself and help transform the future of healthcare , you'll find your purpose here. Job Description: Primary Function of Position: The Financial analyst is responsible for providing analytical support and financial oversight to the leadership team in Mexicali Operations organization, including budget, forecast and actuals analysis; by collecting, monitoring, and studying data and recommending actions. Roles & Responsibilities: • Serve as key analytical and financial partner and advisor to Mexicali Ops and develop tailor-made forecasting and reporting tools (both financial and operational). • Determines cost of operations by establishing standard costs; collecting operational data. • Coordinate Mexicali Ops forecasting, budgeting and month end close ### Packing Operator (Night Shift) - AbbVie Inc. - Location: Westport, MO, Ireland (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012807632-packing-operator-night-shift- - Excerpt: Packing Operator (Night Shift) Westport, MO, Ireland Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: · Maintain a clean and organized work area throughout and at the end of each shift. · Work safely and follow all plant and department health, safety, and environmental policies. · Report safety concerns and observations using the Eachieve system. · Follow all current departmental SOPs and cGMP practices. · Stay up to date with all required cGMP and safety training using ELMS. · Execute packaging tasks to ensure timely product delivery and complete all required documentation. · Set up and clear packaging lines efficiently, preparing equipment and machines for operation in compliance with SOPs and cGMPs. · Troubleshoot equipment issues and work with Maintenance Technicians for mechanical adjustments, reducing downtime and product defects. · Operate and monitor computerized production machinery, maintaining high quality standards. Qualifications: · Leaving Certificate (or equivalent) Additional Information: AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled. US & Puerto Rico ### MSL Reumatología (IBD)- Inmunología - AbbVie Inc. - Location: Remote | Málaga, AN, Spain (remote) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012007926-msl-reumatologia-ibd-inmunologia - Excerpt: MSL Reumatología (IBD)- Inmunología Remote | Málaga, AN, Spain Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Ensure that all activities and interactions are conducted with due regard to all applicable local, global and national laws, regulations, guidelines, codes of conduct, Company policies and accepted standards of best practice. Provide scientific and technical leadership to ensure professional and credible relationships with thought leaders and external experts of strategic importance to AbbVie. Ensure a strong medical and scientific presence for AbbVie in key academic centers by facilitation of research and educational initiatives, while supporting requests for medical and scientific information on products or areas of therapeutic interest to AbbVie. Assist in the initiation; oversight and follow up of assigned clinical studies and medical projects initiated within the therapeutic area for which the MSL carries responsibility (e.g. post marketing clinical activities such as registry/database projects, epidemiological surveys, post-authorization studies (phase IV). All such activities must comply with applicable local laws, guidelines, and codes of practice, SOPs, and AbbVie R&D (GPRD) SOPs. Act as the point of contact with ### Process Safety Lead - AbbVie Inc. - Location: Cork, CO, Ireland (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012196356-process-safety-lead - Excerpt: Process Safety Lead Cork, CO, Ireland Company Description: AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas - immunology, oncology, neuroscience, and eye care - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on X , Facebook , Instagram , YouTube , LinkedIn and Tik Tok . Job Description: We are looking for a Process Safety Lead to join our team in Carraigtwohill, Cork . The Process Safety Lead will be responsible for developing, implementing, managing systems and procedures to prevent major accidents or incidents. You will also be responsible for maintaining and enhancing current systems and ensuring a safe and fit for purpose Process Safety environment. Emergency response and business continuity will also be key areas of responsibility. Roles and Responsibilities Lead the introduction of new products to the site from a process safety perspective. Safe Process Design and Review. Evaluate and design safety systems, including emergency shutdown systems, pressure relief devices (PRDs), fire protection, and explosion prevention systems. Develop and further improve Emergency response and preparedness capabilities. Chair and document process and equipment HAZOP assessments and other process safety related risk assessments and drive follow up actions. Complete Pre-Start Up Safety Reviews (PSSR) in line the relevant Abbvie Technical Standards. Be responsible for process ### Manufacturing Technician ( 12 Month FTC) - AbbVie Inc. - Location: Westport, MO, Ireland (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013532267-manufacturing-technician-12-month-ftc- - Excerpt: Manufacturing Technician ( 12 Month FTC) Westport, MO, Ireland Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: We are now recruiting for Manufacturing Technicians to join our diverse Biologics team in Westport , on a fixed-term contract basis. As our newest technician, you will ensure the highest quality and safety compliance standards while gaining exposure to new and advanced technology in our quality assurance systems. You will also ensure the continued success of our business unit by taking ownership of duties such as compounding, filling and capping of an aseptic product, preparing autoclave loads, testing filters, preparing components, documenting batch related activities, housekeeping and environmental monitoring. PLEASE NOTE: The following role is a 12 hour monthly rotational shift pattern , covering days, nights, weekdays and weekends. If great benefits, a defined career path, and work-life balance are important in your next career move, then read on to find out more. Your Key Activities will include, but are not limited to: Carry out daily tasks as assigned by the Production Manager according to GMP and the quality ### Senior Biotechnologist (Downstream) - AbbVie Inc. - Location: Singapore, , Singapore (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013439506-senior-biotechnologist-downstream- - Excerpt: Senior Biotechnologist (Downstream) Singapore, , Singapore Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Purpose Statement Performs functions associated with cGMP manufacturing operations within the biologics production facility. Completes batch documentation accurately and thoroughly, while adhering to the required quality and safety standards, and in a productive, cost-effective manner. Serves as a highly skilled subject matter expert within the manufacturing area, contributing to the development of concepts, techniques, and process improvements. Supports and drives troubleshooting efforts during course of shift work to ensure adherence to schedule and production plan. Major Responsibilities: To perform purification operations that include column chromatography, tangential flow filtration, Viral filtration and Bulk filling in Glovebox within the biologics production facility Execute on computerized systems (such as Delta V, SAP and MES) for process control and data entry Adhere to safety requirements in all tasks, report incidents and near misses promptly, and assist with Safety, Health, and Environmental (SHE) incident investigations. Participates in resolution of anomalous processing events Assists lead in planning production schedule and leading area activities Performs advance process and equipment ### Aseptic Specialist - AbbVie Inc. - Location: Westport, MO, Ireland (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012764371-aseptic-specialist - Excerpt: Aseptic Specialist Westport, MO, Ireland Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: Purpose: As a member of the Operations function, and as an Aseptic Manufacturing SME, ensures that procedures related to Aseptic Manufacturing follow relevant Regulatory requirements and Network Best Practice. Partners with Site colleagues and other members of the Site Aseptics team, to create an environment of the highest standards of Aseptic Manufacturing. Drives continuous improvement in Aseptic Manufacturing on site. Responsibilities to be added to Job Description (in addition to other duties as assigned) Acts as a site Subject Matter Expert for Aseptic Manufacturing and Microbiology. Responsible for ensuring that Operations procedures required for Aseptic Manufacturing are in compliance with relevant Aseptic and GMP Regulatory requirements and Network Aseptic Best Practice. Ensures appropriate use of Risk Management tools to drive Aseptic performance/ Sterility Assurance. Responsible for completing operability assessments. Partners with other members of the Site Aseptics Team (e.g. Quality SMEs, Engineering SMEs, Aseptic MQA and Aseptic mentors) to ensure required support is provided to manufacturing shifts to ensure safe, quality, and timely ### Packaging Operator - 6 month FTC - AbbVie Inc. - Location: Westport, MO, Ireland (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013442056-packaging-operator-6-month-ftc - Excerpt: Packaging Operator - 6 month FTC Westport, MO, Ireland Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: We are now recruiting Packaging Operators to join our diverse team in Westport, on a 6 Month contract. As our newest operator, you will ensure the highest quality and safety compliance standards while gaining exposure to new and advanced technology in various areas of production, filling and packaging. This role would suit career changers or anyone wishing to gain valuable experience within the pharmaceutical industry. You will operate high-speed equipment for the manual and/or automated assembly and packaging of pharmaceutical products, ensuring adherence to specifications. Flexibility around shifts is essential for these roles as it will include shift support over evenings, nights, and weekends. Is this a team you want to be part of? Then read on… Key Responsibilities: Maintain a clean and organized work area during and at the end of each shift. Assist Abbvie in achieving environmental, health, and safety goals by working safely and observing all general plant and department safety policies. Report safety issues and ### Senior Security Analyst I, Identity & Access Management (Saviynt/Ping) - AbbVie Inc. - Location: Singapore, , Singapore (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013175457-senior-security-analyst-i-identity-access-management-saviynt-ping- - Excerpt: Senior Security Analyst I, Identity & Access Management (Saviynt/Ping) Singapore, , Singapore Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: This position is part of the Information Security & Risk Management (ISRM) team. We are here to put our partners in a position to succeed - providing the knowledge, tools, and governance frameworks they need to use data and technology securely while managing risk at enterprise scale. We are looking for a highly motivated, technically skilled identity professional to join our Identity and Access Management (IAM) team. This role is critical in safeguarding the enterprise by ensuring that user access is accurate, compliant, and aligned with global security standards. The IAM Senior Security Analyst I will drive the full lifecycle of identity governance across OIM, Saviynt, Ping, Active Directory, and other enterprise identity systems - enabling secure, seamless access for employees, contractors, and partners worldwide. The ideal candidate brings deep hands-on expertise in identity administration and governance, a strong understanding of compliance frameworks, and the ability to work independently to drive improvements across people, processes, and ### Supervisor, Laboratory Quality Control - AbbVie Inc. - Location: Dublin, County Dublin, Ireland (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990012613671-supervisor-laboratory-quality-control - Excerpt: Supervisor, Laboratory Quality Control Dublin, County Dublin, Ireland Company Description: About AbbVie AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com . Follow @abbvie on LinkedIn, Facebook , Instagram , X and YouTube. Job Description: We are now hiring a QC Supervisor to join our team on our site in North Dublin. The QC Supervisor is a key member of the Quality Control team, responsible for leading day-to-day quality control laboratory operations and ensuring effective support for QA, Technical Service, and Production in line with site schedules and targets. This role supervises a team of QC Chemists, reports to the QC Manager, and may act as deputy when required. The position requires strong leadership, technical expertise, and a commitment to compliance with all applicable laws, regulations, company policies, and cGMP standards. Responsibilities Supervise daily QC laboratory operations and ensure work is performed in accordance with regulatory and company requirements. Support daily and weekly production schedules, including participation in Tier 1 and Tier 2 meetings. Escalate laboratory, safety, equipment, process, and systems issues through the site escalation process as needed. Lead, coach, and develop QC staff to build capability, support performance, and strengthen succession planning. Ensure ### Manager Manufacturing Engineering - Intuitive Surgical, Inc. - Location: Mexicali, MEXICO, Mexico (unspecified) - Salary: Not disclosed - Posted: 2026-06-12 - Parental leave: 8 weeks (not source-backed) - Non-birth-parent leave: 8 weeks (not source-backed) - Apply: https://jobs.smartrecruiters.com/Intuitive/744000129776171-manager-manufacturing-engineering - Excerpt: Manager Manufacturing Engineering Mexicali, MEXICO, Mexico Company Description: It started with a simple idea: what if surgery could be less invasive and recovery less painful? Nearly 30 years later, that question still fuels everything we do at Intuitive . As a global leader in robotic-assisted surgery and minimally invasive care , our technologies-like the da Vinci surgical system and Ion -have transformed how care is delivered for millions of patients worldwide. We're a team of engineers, clinicians, and innovators united by one purpose: to make surgery smarter, safer, and more human. Every day, our work helps care teams perform with greater precision and patients recover faster, improving outcomes around the world. The problems we solve demand creativity, rigor, and collaboration. The work is challenging, but deeply meaningful-because every improvement we make has the potential to change a life. If you're ready to contribute to something bigger than yourself and help transform the future of healthcare , you'll find your purpose here. Job Description: Primary Function of Position: To define and execute the strategy for the Manufacturing Engineering area that will promote the continuous improvement and support to released production processes for Instruments and Accessories to ensure reliability, cost, manufacturability and serviceability. To manage and coordinate the resources and activities of the Manufacturing Engineer area and provide mechanical and manufacturing support in accordance with FDA 21 CFR820 and ISO 13485 standard regulations. Define budget of the department and execute as planned. This position requires minimal to no supervision. Roles & Responsibilities: ### Maintenance Manager (all genders) - Vollzeit, unbefristet - AbbVie Inc. - Location: Ludwigshafen, RP, Germany (unspecified) - Salary: Not disclosed - Posted: 2026-06-10 - Parental leave: 12 weeks (not source-backed) - Non-birth-parent leave: 12 weeks (not source-backed) - 401(k) match: listed (source-backed) - Source: https://www.askebsa.dol.gov/FOIA%20Files/2024/Latest/F_SCH_H_2024_Latest.zip - Apply: https://jobs.smartrecruiters.com/AbbVie/3743990010711156-maintenance-manager-all-genders-vollzeit-unbefristet - Excerpt: Maintenance Manager (all genders) - Vollzeit, unbefristet Ludwigshafen, RP, Germany Company Description: Welcome to AbbVie! As part of an international company with 50,000 employees worldwide and around 3,000 employees in Germany, you will have the opportunity of addressing some of tomorrows unmet medical needs in close collaboration with your colleagues. Are you passionate about improving global health care? Do you want to contribute to improving patients' quality of life through your expertise? In a challenging work environment that offers opportunities of developing and increasing your own skills? You've come to the right place! For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok. Job Description: Moving mountains together - as Maintenance Manager (all genders) you are responsible for technical availability of manufacturing, packaging and logistics equipment. You are developing strategies for organization and execution of maintenance program for operations in compliance with applicable policies and procedures. Your main responsibilities: • Evaluation and optimization of equipment, technical standards and manufacturing processes • Develop strategies and execute global Maintenance Excellence Program • Manage multiple, often concurrent site projects/programs • Support site project/program strategy to align and achieve key customer business objectives • Anticipates trends and business needs and prioritize accordingly • Develops departmental plans, including business, production and/or organizational priorities • Controls resources and policy formation in area of responsibility • Active role in planning, monitoring and control of investment budgets • Provide leadership to managers, supervisors and/or professional staff Qualifications: --- Source-backed benefit claims include source links; other benefit values are labeled separately.