Standard Biotools Inc jobs

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 US-AZ-TUCSON-802 ~ 1151 E Hermans Rd ~ BLDG 802 posted: Posted 30+ Days Ago

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) US-FL-JUPITER-MFG ~ 17900 Beeline Hwy ~ MFG BLDG posted: Posted 30+ Days Ago

Bus Exp & Plan Advisor - Physical Security Products and Standards 5 Locations posted: Posted 10 Days Ago

Associate Director - Quality Standards and Continuous Improvement Uxbridge1 posted: Posted 3 Days Ago

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 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 Longmont posted: Posted 30+ Days Ago

Director, Program Management Process and Standards 2 Locations posted: Posted 4 Days Ago

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

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,

Quality Specialist - Industry Standards Compliance HU-PE-FOT-EAST GATE BUSINESS PARK posted: Posted 4 Days Ago

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

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

Lead Engineer - Technical Regulations & Standards Greenville posted: Posted 30 Days Ago

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.

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 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 3 Locations posted: Posted 10 Days Ago

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

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,

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

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,