# FewerJobs export - 100 curated jobs
Generated: 2026-08-15T07:11:05.423Z
Source: https://fewerjobs.com

## Filters applied
- **q**: ORIC Pharmaceuticals
- **quality_floor**: default
- **match_401k_strict**: true
- **parental_strict**: true
- **non_birth_strict**: true
- **pto_strict**: true
- **include_older**: false
- **apply_url_verified**: false
- **page**: 1
- **per_page**: 100
- **sort**: relevance

## Jobs
### Regulatory Affairs Manager - ORIC Pharmaceuticals
- Location: San Diego, CA, United States (unspecified)
- Salary: $145K-$165K
- Posted: 2026-06-10
- Apply: https://jobs.smartrecruiters.com/ORICPharmaceuticals/3743990012420696-regulatory-affairs-manager
- Excerpt: Regulatory Affairs Manager San Diego, CA, United States Company Description: ORIC Pharmaceuticals is a clinical stage biopharmaceutical company dedicated to improving patients' lives by Overcoming Resistance In Cancer. ORIC's clinical stage product candidates include (1) ORIC-944, an allosteric inhibitor of the polycomb repressive complex 2 (PRC2) via the EED subunit, being developed for prostate cancer, and (2) ORIC-114, a brain penetrant inhibitor that selectively targets EGFR exon 20, HER2 exon 20 and EGFR atypical mutations, being developed across multiple genetically defined cancers. Beyond these two product candidates, ORIC® is also developing multiple precision medicines targeting other hallmark cancer resistance mechanisms. ORIC has offices in South San Francisco and San Diego, California. Job Description: We are seeking a motivated Regulatory Affairs professional to join our team and help advance the clinical development of oncology products at ORIC. In this role, you will collaborate closely with colleagues across regulatory operations, quality, CMC, nonclinical and clinical functions to support high-quality, timely regulatory submissions. The ideal candidate is a proactive team player who thrives in cross-functional environments, communicates effectively, and can balance strategic thinking with strong execution. Essential duties and responsibilities include the following. Other duties may be assigned. Support regulatory submissions and contribute to strategic planning for assigned programs. Prepare and deliver high-quality and timely regulatory submissions in compliance with applicable regulatory requirements. Responsible for the creation, assembly, review, and archival of complex regulatory submissions which require interaction with internal and CRO teams to ensure optimal execution. Develop, manage and track regulatory submission

### Senior Scientist, Analytical Sciences - ORIC Pharmaceuticals
- Location: South San Francisco, CA, United States (unspecified)
- Salary: $150K-$180K
- Posted: 2026-06-10
- Apply: https://jobs.smartrecruiters.com/ORICPharmaceuticals/3743990011640247-senior-scientist-analytical-sciences
- Excerpt: Senior Scientist, Analytical Sciences South San Francisco, CA, United States Company Description: ORIC Pharmaceuticals is a clinical stage biopharmaceutical company dedicated to improving patients' lives by Overcoming Resistance In Cancer. ORIC's clinical stage product candidates include (1) rinzimetostat (ORIC-944), an allosteric inhibitor of the polycomb repressive complex 2 (PRC2) via the EED subunit, being developed for prostate cancer, and (2) enozertinib, a brain penetrant inhibitor that selectively targets EGFR exon 20, HER2 exon 20 and EGFR atypical mutations, being developed across multiple genetically defined cancers. Beyond these two product candidates, ORIC® is also developing multiple precision medicines targeting other hallmark cancer resistance mechanisms. ORIC has offices in South San Francisco and San Diego, California. For more information, please go to www.oricpharma.com , and follow us on X or LinkedIn . We are seeking a lab-based, highly motivated Senior Scientist in Analytical Sciences. The candidate will be part of cross-functional teams providing analytical leadership on projects, work closely on a shared mission to bring new therapeutics to cancer patients. The successful candidate will report to the Sr. Director of Analytical Sciences Job Description: Independently lead analytical development and product characterization activities for our drug development portfolios. Provide oversight, technical guidance and tactical direction for analytical method development, transfer, validation, release, and stability testing activities at CDMOs. Function as a subject matter expert for in-depth physical/ chemical characterization of NCEs at CROs. Independently conceptualize, design, and conduct experiments; interpret and present data and conclusions to various audience, including senior leadership. Expected to

### Senior Scientist, Process Chemistry - ORIC Pharmaceuticals
- Location: South San Francisco, CA, United States (unspecified)
- Salary: $175K-$200K
- Posted: 2026-06-10
- Apply: https://jobs.smartrecruiters.com/ORICPharmaceuticals/3743990013454986-senior-scientist-process-chemistry-
- Excerpt: Senior Scientist, Process Chemistry South San Francisco, CA, United States Company Description: ORIC Pharmaceuticals is a clinical stage biopharmaceutical company dedicated to improving patients' lives by Overcoming Resistance In Cancer. ORIC's clinical stage product candidates include (1) ORIC-944, an allosteric inhibitor of the polycomb repressive complex 2 (PRC2) via the EED subunit, being developed for prostate cancer, and (2) ORIC-114, a brain penetrant inhibitor that selectively targets EGFR exon 20, HER2 exon 20 and EGFR atypical mutations, being developed across multiple genetically defined cancers. Beyond these two product candidates, ORIC® is also developing multiple precision medicines targeting other hallmark cancer resistance mechanisms. ORIC has offices in South San Francisco and San Diego, California. We are seeking a highly motivated process development and chemistry senior scientist. This senior scientist designs and executes multi-step experimental studies, utilizing analytical tools to ensure safe and scalable processes. They collaborate cross-functionally, author technical reports, and facilitate the transfer of technology for GMP manufacturing. Job Description: Design, planning, and execution of multi-step experimental studies to provide safe, efficient, robust and scalable processes. Independently use PAT and analytical tools and interpret data to gain reaction understanding. Share literature and available resources to support relevant precedent for process research. Perform experiments and interpret data (calorimetry, TGA, DSC) to safely scale reactions. Author development reports and technical packages, and author/review relevant sections in health authority filings (including INDs, NDAs, annual reports, and any other regulatory interactions) and patents. Prepare presentation materials and clearly communicate research results to manager, and

### Director, Medical Affairs - ORIC Pharmaceuticals
- Location: South San Francisco, CA, United States | Remote (remote)
- Salary: $220K-$275K
- Posted: 2026-06-10
- Apply: https://jobs.smartrecruiters.com/ORICPharmaceuticals/3743990013504016--director-medical-affairs
- Excerpt: Director, Medical Affairs South San Francisco, CA, United States | Remote Company Description: ORIC Pharmaceuticals is a clinical stage biopharmaceutical company dedicated to improving patients' lives by Overcoming Resistance In Cancer. ORIC's clinical stage product candidates include (1) rinzimetostat (ORIC-944), an allosteric inhibitor of the polycomb repressive complex 2 (PRC2) via the EED subunit, being developed for prostate cancer, and (2) enozertinib, a brain penetrant inhibitor that selectively targets EGFR exon 20, HER2 exon 20 and EGFR atypical mutations, being developed across multiple genetically defined cancers. Beyond these two product candidates, ORIC® is also developing multiple precision medicines targeting other hallmark cancer resistance mechanisms. ORIC has offices in South San Francisco and San Diego, California. For more information, please go to www.oricpharma.com , and follow us on X or LinkedIn . ORIC Pharmaceuticals is seeking a Director, Medical Affairs, as a member of the Global Medical Affairs (GMA) team based in ORIC's South San Francisco office. Reporting to the Head of Medical Affairs, this individual will be responsible for developing and executing the GMA strategy and tactical plans with a focus on launch readiness and life cycle management for therapies across prostate cancer, non-small cell lung cancer (NSCLC), and potentially other tumor types. The successful candidate will have a proven track record of developing and driving medical strategy for multiple assets with a focus on effectively analyzing and communicating key scientific data through publications, medical information, medical communications, congress activities as well as gathering insights through advisory boards, advocacy, and

### People Operations Specialist (Contract) - ORIC Pharmaceuticals
- Location: San Diego, CA, United States (unspecified)
- Salary: $40-$45/hr
- Posted: 2026-06-10
- Apply: https://jobs.smartrecruiters.com/ORICPharmaceuticals/3743990013155012-people-operations-specialist-contract-
- Excerpt: People Operations Specialist (Contract) San Diego, CA, United States Company Description: ORIC Pharmaceuticals is a clinical stage biopharmaceutical company dedicated to improving patients' lives by Overcoming Resistance In Cancer. ORIC's clinical stage product candidates include (1) Rinzimetostat (ORIC-944), an allosteric inhibitor of the polycomb repressive complex 2 (PRC2) via the EED subunit, being developed for prostate cancer, and (2) Enozertinib (ORIC-114), a brain penetrant inhibitor that selectively targets EGFR exon 20, HER2 exon 20 and EGFR atypical mutations, being developed across multiple genetically defined cancers. Beyond these two product candidates, ORIC® is also developing multiple precision medicines targeting other hallmark cancer resistance mechanisms. ORIC has offices in South San Francisco and San Diego, California. ORIC's People Team is looking for a highly motivated People Operations Specialist to support key initiatives and the day-to-day operations of the People Team. This position will play a crucial role in creating a positive candidate and employee experience and maintaining ORIC as a best place to work for all our team members. This includes supporting the full set of employment lifecycle activities, ensuring a seamless experience for employees, managers, and the People and Payroll teams. The ideal candidate can manage multiple responsibilities and projects effectively and efficiently and is keenly interested in learning and developing in the field of Human Resources. Job Description: Talent Acquisition (60%) Schedule candidate seminars and interviews; create interview agendas and host on-site interviews as required Coordinate travel, meals, and candidate expenses Create and monitor onboarding and offboarding checklists for completion

### Medical Director/Senior Medical Director, Clinical Development (Prostate) - ORIC Pharmaceuticals
- Location: San Diego, CA, United States (unspecified)
- Salary: $270K-$320K
- Posted: 2026-06-10
- Apply: https://jobs.smartrecruiters.com/ORICPharmaceuticals/3743990013417826-medical-director-senior-medical-director-clinical-development-prostate-
- Excerpt: Medical Director/Senior Medical Director, Clinical Development (Prostate) San Diego, CA, United States Company Description: ORIC Pharmaceuticals is a clinical stage biopharmaceutical company dedicated to improving patients' lives by Overcoming Resistance In Cancer. ORIC's clinical stage product candidates include (1) rinzimetostat, an allosteric inhibitor of the polycomb repressive complex 2 (PRC2) via the EED subunit, being developed for prostate cancer, and (2) enozertinib, a brain penetrant inhibitor that selectively targets EGFR exon 20, HER2 exon 20 and EGFR atypical mutations, being developed across multiple genetically defined cancers. Beyond these two product candidates, ORIC® is also developing multiple precision medicines targeting other hallmark cancer resistance mechanisms. ORIC has offices in South San Francisco and San Diego, California. For more information, please go to www.oricpharma.com , and follow us on X or LinkedIn . We are seeking an experienced oncology physician to serve as a Medical Director or Senior Medical Director at ORIC Pharmaceuticals. This role provides medical leadership across one or more clinical development programs, with a primary focus on late-stage (registration-enabling) clinical trials. The position plays a critical role in shaping clinical strategy, ensuring scientific rigor, guiding regulatory interactions, and advancing programs from study design through regulatory submission. The Medical Director will work in close partnership with cross-functional teams including Clinical Operations, Regulatory Affairs, Biostatistics, Safety/Pharmacovigilance, Translational Medicine, and Medical Affairs. The role requires strong strategic thinking, hands-on execution, and the ability to lead effectively in a fast-paced biotech environment. Job Description: Clinical and Medical Leadership Serve as the medical lead

### Director, Clinical Quality Assurance - ORIC Pharmaceuticals
- Location: San Diego, CA, United States (unspecified)
- Salary: $200K-$220K
- Posted: 2026-06-10
- Apply: https://jobs.smartrecruiters.com/ORICPharmaceuticals/3743990012293946-director-clinical-quality-assurance-
- Excerpt: Director, Clinical Quality Assurance San Diego, CA, United States Company Description: ORIC Pharmaceuticals is a clinical stage biopharmaceutical company dedicated to improving patients' lives by Overcoming Resistance In Cancer. ORIC's clinical stage product candidates include (1) rinzimetostat (ORIC-944), an allosteric inhibitor of the polycomb repressive complex 2 (PRC2) via the EED subunit, being developed for prostate cancer, and (2) enozertinib, a brain penetrant inhibitor that selectively targets EGFR exon 20, HER2 exon 20 and EGFR atypical mutations, being developed across multiple genetically defined cancers. Beyond these two product candidates, ORIC® is also developing multiple precision medicines targeting other hallmark cancer resistance mechanisms. ORIC has offices in South San Francisco and San Diego, California. For more information, please go to www.oricpharma.com , and follow us on X or LinkedIn . Reporting to the Senior Vice President of Quality, the Director of Clinical Quality Assurance will lead the Clinical QA function and provide strategic leadership and operational oversight across global early to late-stage clinical programs. The role is responsible for the development, implementation and oversight of quality policies, procedures, and risk-based systems appropriate for advancement of clinical programs. This individual will ensure compliance with global regulatory regulations, as applicable. The successful candidate will work closely with Clinical Development, Clinical Operations, Regulatory Affairs, and third-party Contract organizations to prepare the team for BLA/BIMO milestones. An in-depth understanding of global Health Authority requirements, clinical program management, quality systems, validation, and data integrity are essential requirements of the role. Job Description: Ensure compliance with all

### Senior Director, Quality - ORIC Pharmaceuticals
- Location: San Diego, CA, United States (unspecified)
- Salary: $220K-$270K
- Posted: 2026-06-10
- Apply: https://jobs.smartrecruiters.com/ORICPharmaceuticals/3743990011995852-senior-director-quality-
- Excerpt: Senior Director, Quality San Diego, CA, United States Company Description: ORIC Pharmaceuticals is a clinical stage biopharmaceutical company dedicated to improving patients' lives by Overcoming Resistance In Cancer. ORIC's clinical stage product candidates include (1) rinzimetostat (ORIC-944), an allosteric inhibitor of the polycomb repressive complex 2 (PRC2) via the EED subunit, being developed for prostate cancer, and (2) enozertinib, a brain penetrant inhibitor that selectively targets EGFR exon 20, HER2 exon 20 and EGFR atypical mutations, being developed across multiple genetically defined cancers. Beyond these two product candidates, ORIC® is also developing multiple precision medicines targeting other hallmark cancer resistance mechanisms. ORIC has offices in South San Francisco and San Diego, California. For more information, please go to www.oricpharma.com , and follow us on X or LinkedIn . Reporting to the Senior Vice President of Quality, the Sr. Director of Quality will lead provide quality oversight of clinical development and manufacturing programs. This individual will lead the Chemistry, Manufacturing, and Controls (CMC) QA team and provide end-to-end development to manufacturing support for clinical stage programs and will develop systems to commercialize late-stage assets. This position will design, develop, and implement clinical and commercial quality strategies to ensure appropriate compliance to applicable regulatory regulations. The successful candidate will work closely with Technical Operations, Regulatory Affairs, and third-party Contract Development and Manufacturing Organizations (CDMOs) and will be responsible for all levels of studies, ranging from simple to complex and requires an in-depth understanding of GMPs, global Health Authority requirements, program management, quality

### Associate Director, CMC Project Management - ORIC Pharmaceuticals
- Location: South San Francisco, CA, United States (unspecified)
- Salary: $210K-$260K
- Posted: 2026-06-10
- Apply: https://jobs.smartrecruiters.com/ORICPharmaceuticals/3743990013501357-associate-director-cmc-project-management
- Excerpt: Associate Director, CMC Project Management South San Francisco, CA, United States Company Description: ORIC Pharmaceuticals is a clinical stage biopharmaceutical company dedicated to improving patients' lives by Overcoming Resistance In Cancer. ORIC's clinical stage product candidates include (1) rinzimetostat (ORIC-944), an allosteric inhibitor of the polycomb repressive complex 2 (PRC2) via the EED subunit, being developed for prostate cancer, and (2) enozertinib, a brain penetrant inhibitor that selectively targets EGFR exon 20, HER2 exon 20 and EGFR atypical mutations, being developed across multiple genetically defined cancers. Beyond these two product candidates, ORIC® is also developing multiple precision medicines targeting other hallmark cancer resistance mechanisms. ORIC has offices in South San Francisco and San Diego, California. For more information, please go to www.oricpharma.com , and follow us on X or LinkedIn . This role requires a leader with strong business acumen to define and execute business processes that drive complex programs through global registration and commercialization. This role will play a pivotal part in bringing innovative therapies to patients by ensuring that CMC development, manufacturing, and commercialization are executed with excellence, speed, and financial discipline. This individual will also oversee project management including timelines, budgets, invoices, reports and documentation, and may assist with regulatory filings. This position reports to the Chief Technical Officer and is responsible for the following: Job Description: 1. End-to-End CMC Leadership & Cross-Functional Integration Create and execute against integrated cross-functional project plans, leading the integrated CMC strategy. Translate program strategy into cohesive development, manufacturing, and supply plans

### Senior Manager, Pharmacovigilance - ORIC Pharmaceuticals
- Location: San Diego, CA, United States | Remote (remote)
- Salary: $150K-$180K
- Posted: 2026-06-10
- Apply: https://jobs.smartrecruiters.com/ORICPharmaceuticals/3743990011886996-senior-manager-pharmacovigilance
- Excerpt: Senior Manager, Pharmacovigilance San Diego, CA, United States | Remote Company Description: ORIC Pharmaceuticals is a clinical stage biopharmaceutical company dedicated to improving patients' lives by Overcoming Resistance In Cancer. ORIC's clinical stage product candidates include (1) rinzimetostat (ORIC-944), an allosteric inhibitor of the polycomb repressive complex 2 (PRC2) via the EED subunit, being developed for prostate cancer, and (2) enozertinib, a brain penetrant inhibitor that selectively targets EGFR exon 20, HER2 exon 20 and EGFR atypical mutations, being developed across multiple genetically defined cancers. Beyond these two product candidates, ORIC® is also developing multiple precision medicines targeting other hallmark cancer resistance mechanisms. ORIC has offices in South San Francisco and San Diego, California. For more information, please go to www.oricpharma.com , and follow us on X or LinkedIn . The Senior Manager of Pharmacovigilance will be responsible for the execution of global pharmacovigilance activities supporting late-stage clinical development and preparation for first commercial launch of small-molecule oncology products in lung and prostate cancer. This role will ensure compliance with global safety regulations and will work closely with cross-functional partners to ensure individual case safety report (ICSR) processing, Health Authority submissions, and post-marketing safety readiness. This is a hands-on role well suited for a biotech environment requiring both operational excellence and cross-functional collaboration. Job Description: Global Drug Safety & Pharmacovigilance Operations Manage end-to-end pharmacovigilance activities for clinical trials and post-approval oncology products In partnership with Clinical Research Organizations (CROs), oversee intake, assessment, processing, medical review, and reporting of ICSRs from

### Senior Director, CMC Program Management - ORIC Pharmaceuticals
- Location: South San Francisco, CA, United States (unspecified)
- Salary: $275K-$310K
- Posted: 2026-06-10
- Apply: https://jobs.smartrecruiters.com/ORICPharmaceuticals/3743990013359367-senior-director-cmc-program-management
- Excerpt: Senior Director, CMC Program Management South San Francisco, CA, United States Company Description: ORIC Pharmaceuticals is a clinical stage biopharmaceutical company dedicated to improving patients' lives by Overcoming Resistance In Cancer. ORIC's clinical stage product candidates include (1) rinzimetostat (ORIC-944), an allosteric inhibitor of the polycomb repressive complex 2 (PRC2) via the EED subunit, being developed for prostate cancer, and (2) enozertinib, a brain penetrant inhibitor that selectively targets EGFR exon 20, HER2 exon 20 and EGFR atypical mutations, being developed across multiple genetically defined cancers. Beyond these two product candidates, ORIC® is also developing multiple precision medicines targeting other hallmark cancer resistance mechanisms. ORIC has offices in South San Francisco and San Diego, California. For more information, please go to www.oricpharma.com , and follow us on X or LinkedIn . This role requires a leader with strong business acumen to define and execute business processes that drive complex programs through global registration and commercialization. This role will play a pivotal part in bringing innovative therapies to patients by ensuring that CMC development, manufacturing, and commercialization are executed with excellence, speed, and financial discipline. This individual will also oversee project management including timelines, budgets, invoices, reports and documentation, and may assist with regulatory filings. This position reports to the Chief Technical Officer and is responsible for the following: Job Description: 1. End-to-End CMC Leadership & Cross-Functional Integration Create and execute against integrated cross-functional project plans, leading the integrated CMC strategy. Translate program strategy into cohesive development, manufacturing, and supply plans

### Senior Director/ Director, CMC Regulatory Affairs - ORIC Pharmaceuticals
- Location: South San Francisco, CA, United States (unspecified)
- Salary: $220K-$300K
- Posted: 2026-06-10
- Apply: https://jobs.smartrecruiters.com/ORICPharmaceuticals/3743990010682796-senior-director-director-cmc-regulatory-affairs
- Excerpt: Senior Director/ Director, CMC Regulatory Affairs South San Francisco, CA, United States Company Description: ORIC Pharmaceuticals is a clinical stage biopharmaceutical company dedicated to improving patients' lives by Overcoming Resistance In Cancer. ORIC's clinical stage product candidates include (1) ORIC-944, an allosteric inhibitor of the polycomb repressive complex 2 (PRC2) via the EED subunit, being developed for prostate cancer, and (2) enozertinib (ORIC-114), a brain penetrant inhibitor that selectively targets EGFR exon 20, HER2 exon 20 and EGFR atypical mutations, being developed across multiple genetically defined cancers. ORIC has offices in South San Francisco and San Diego, California. For more information, please go to www.oricpharma.com , and follow us on X or LinkedIn . Reporting to the Chief Technical Officer, we are currently hiring a Director, CMC Regulatory Affairs, to join our Technical Operations team. This position is responsible for leading CMC regulatory activities and supporting all of ORIC's clinical development programs for oncology products. The role involves close collaboration with cross-functional teams including regulatory affairs, regulatory operations, quality, CMC, nonclinical, and clinical departments. Job Description: Oversee and direct all CMC regulatory strategies in compliance with global regulatory requirements for the development of ORIC's products. Provide CMC regulatory support for new and ongoing clinical trials, e.g., manage/prepare CMC document packages in support of INDs, CTAs and amendments to global regulatory agencies (RAs) and health authorities (HAs) Work collaboratively with Pharmaceutical Development, Drug Substance, and GMP Quality Assurance, in addition to Project Management, Clinical Operations, Clinical Supply, and Regulatory Operations. Lead

### Principal or Associate Scientist, Analytical Development Japan, Pharmaceutical Sciences - Takeda Pharmaceutical Company Limited
- Location: Fujisawa, Japan (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- 401(k) match: listed (not source-backed)
- Apply: https://takeda.wd3.myworkdayjobs.com/External/job/Fujisawa-Japan/Principal-or-Associate-Scientist--Analytical-Development-Japan--Pharmaceutical-Sciences_R0177837-1
- Excerpt: Principal or Associate Scientist, Analytical Development Japan, Pharmaceutical Sciences Fujisawa, Japan posted: Posted 30+ Days Ago

### Associate Director or Principal Scientist, Facility Operations, Pharmaceutical Sciences - Takeda Pharmaceutical Company Limited
- Location: Fujisawa, Japan (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- 401(k) match: listed (not source-backed)
- Apply: https://takeda.wd3.myworkdayjobs.com/External/job/Fujisawa-Japan/Associate-Director-or-Principal-Scientist--Facility-Operations--Pharmaceutical-Sciences_R0178525-1
- Excerpt: Associate Director or Principal Scientist, Facility Operations, Pharmaceutical Sciences Fujisawa, Japan posted: Posted 30+ Days Ago

### Pharmaceutical Sciences, Technology & Innovation Lead (Sr. Director) - Takeda Pharmaceutical Company Limited
- Location: Boston, MA (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-11
- 401(k) match: listed (not source-backed)
- Apply: https://takeda.wd3.myworkdayjobs.com/External/job/Boston-MA/Pharmaceutical-Sciences--Technology---Innovation-Lead--Sr-Director-_R0178501-1
- Excerpt: Pharmaceutical Sciences, Technology & Innovation Lead (Sr. Director) Boston, MA posted: Posted Yesterday

### Pharmaceutical Sciences, Operations & Performance Lead (Sr. Director) - Takeda Pharmaceutical Company Limited
- Location: Boston, MA (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- 401(k) match: listed (not source-backed)
- Apply: https://takeda.wd3.myworkdayjobs.com/External/job/Boston-MA/Pharmaceutical-Sciences--Strategy---Operations-Lead--Sr-Director-_R0178498
- Excerpt: Pharmaceutical Sciences, Operations & Performance Lead (Sr. Director) Boston, MA posted: Posted 30+ Days Ago

### Pharmaceutical Technician II - Thermo Fisher Scientific
- Location: Singapore, Singapore (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-11
- 401(k) match: listed (not source-backed)
- Apply: https://thermofisher.wd5.myworkdayjobs.com/ThermoFisherCareers/job/Singapore-Singapore/Pharmaceutical-Technician-II_R-01354187/apply
- Excerpt: Pharmaceutical Technician II Singapore, Singapore Embrace the role of a Pharmaceutical Technician II and play a vital role in sterile pharmaceutical production. Operate advanced equipment, ensure GMP compliance, and support quality manufacturing processes. If you have hands-on experience in pharmaceutical manufacturing and a passion for safety and precision, this is your opportunity to make an impact.

### Pharmaceutical Technician II - Thermo Fisher Scientific
- Location: Singapore, Singapore (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-11
- 401(k) match: listed (not source-backed)
- Apply: https://thermofisher.wd5.myworkdayjobs.com/ThermoFisherCareers/job/Singapore-Singapore/Pharmaceutical-Technician-II_R-01349946-1/apply
- Excerpt: Pharmaceutical Technician II Singapore, Singapore Embrace the role of a Pharmaceutical Technician II and play a vital role in sterile pharmaceutical production. Operate advanced equipment, ensure GMP compliance, and support quality manufacturing processes. Ideal for candidates with 1-5 years' experience in pharma, this role offers hands-on work in a dynamic, safety-focused environment. Grow your career in pharmaceutical manufacturing today!

### Pharmaceutical Technician II - Thermo Fisher Scientific
- Location: Singapore, Singapore (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-11
- 401(k) match: listed (not source-backed)
- Apply: https://thermofisher.wd5.myworkdayjobs.com/ThermoFisherCareers/job/Singapore-Singapore/Pharmaceutical-Technician-II_R-01340678/apply
- Excerpt: Pharmaceutical Technician II Singapore, Singapore Embrace the role of a Pharmaceutical Technician II and play a vital role in sterile pharmaceutical production. Operate advanced equipment, ensure GMP compliance, and contribute to quality manufacturing. If you have hands-on experience in pharma production and a passion for safety and precision, this is your opportunity to make a difference.

### Pharmaceutical Technician II - Thermo Fisher Scientific
- Location: Singapore, Singapore (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-11
- 401(k) match: listed (not source-backed)
- Apply: https://thermofisher.wd5.myworkdayjobs.com/ThermoFisherCareers/job/Singapore-Singapore/Pharmaceutical-Technician-II_R-01340680-1/apply
- Excerpt: Pharmaceutical Technician II Singapore, Singapore Embrace the opportunity to become a Pharmaceutical Technician II and play a vital role in sterile pharmaceutical production. Operate advanced equipment, ensure GMP compliance, and contribute to quality manufacturing. If you have hands-on experience in pharma production and a passion for safety and precision, this is your opportunity to make a difference.

### Director / Senior Director, Regulatory CMC (Biologics) - Oruka Therapeutics Inc
- Location: Waltham, Massachusetts, United States (unspecified)
- Salary: $213K-$286K
- Posted: 2026-04-10
- Apply: https://job-boards.greenhouse.io/oruka/jobs/5184371008
- Excerpt: Director / Senior Director, Regulatory CMC (Biologics) Waltham, Massachusetts, United States About Us: Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture. Job Title: Director / Senior Director, Regulatory CMC (Biologics) Location: Hybrid - Waltham, MA Candidates will be required to be in-office 3 days/week. Role Overview: We are seeking an experienced and motivated regulatory CMC leader to shape strategy and execution across early-to-late-stage biologics programs. In this role, you will own the development of high-quality regulatory CMC submissions and guide cross-functional teams on phase-appropriate global regulatory expectations. You are an ideal candidate if you bring deep expertise in biologics development and manufacturing, including strong experience with drug substance and drug product

### Pharmaceutical Sales Specialist Immunology - Alsace - Regeneron Pharmaceuticals
- Location: Remote - France (remote)
- 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 (not source-backed)
- Apply: https://regeneron.wd1.myworkdayjobs.com/Careers/job/Remote---France/Pharmaceutical-Sales-Specialist-Immunology---Alsace_R47580
- Excerpt: Pharmaceutical Sales Specialist Immunology - Alsace Remote - France posted: Posted 4 Days Ago

### Executive Medical Director, Clinical Development - Oruka Therapeutics Inc
- Location: Menlo Park, California, United States; Remote; Waltham, Massachusetts, United States (remote)
- Salary: $331K-$368K
- Posted: 2026-04-30
- Hires in: CA, MA
- Apply: https://job-boards.greenhouse.io/oruka/jobs/5206495008
- Excerpt: Executive Medical Director, Clinical Development Menlo Park, California, United States; Remote; Waltham, Massachusetts, United States About Us: Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture. Job Title: Executive Medical Director, Clinical Development Location: Remote OR Hybrid 3 days/week if located near office in either Waltham, MA or Menlo Park, CA will be required. . Role Overview: The Executive Medical Director of Clinical Development plays a key role in leading the design, execution, and oversight of clinical trials at an asset level, ensuring high-quality data generation to support the safety and efficacy of our pipeline products. This role involves leading and developing a team and contributing to and influencing clinical development strategy

### Director, Clinical Monitoring Strategy - Oruka Therapeutics Inc
- Location: Menlo Park, California, United States; Remote; Waltham, Massachusetts, United States (remote)
- Salary: $213K-$240K
- Posted: 2026-05-29
- Apply: https://job-boards.greenhouse.io/oruka/jobs/5236397008
- Excerpt: Director, Clinical Monitoring Strategy Menlo Park, California, United States; Remote; Waltham, Massachusetts, United States About Us: Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture. Job Title: Director, Clinical Monitoring Strategy and Optimization Location: Remote or Waltham, MA or Menlo Park, CA, Hybrid - onsite up to 3 days/week is required when not traveling. Role Overview: We are seeking an experienced and highly motivated Director of Clinical Monitoring Strategy and Optimization to provide strategic and operational leadership for clinical monitoring activities across our development programs. This individual will play a critical role in building and scaling clinical operations infrastructure within a fast-paced emerging biotech environment. The successful candidate will oversee CRO monitoring

### Director, Quality Control - Oruka Therapeutics Inc
- Location: Menlo Park, California, United States; Remote; Waltham, Massachusetts, United States (remote)
- Salary: $213K-$240K
- Posted: 2026-05-28
- Apply: https://job-boards.greenhouse.io/oruka/jobs/5234803008
- Excerpt: Director, Quality Control Menlo Park, California, United States; Remote; Waltham, Massachusetts, United States About Us: Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture. Job Title: Director, Quality Control Location: Hybrid - Waltham, MA or Menlo Park, CA. Candidates will be required to be in-office 3 days/week Open to remote for non-local candidates. Role Overview: The Director, Quality Control - Combination Products will provide strategic and operational leadership for the Quality Control function supporting late-stage clinical development, analytical testing oversight for clinical drug substance and drug product, process performance qualification (PPQ), regulatory submissions, and commercial launch readiness for monoclonal antibody drug products and combination products, including pre-filled syringes and autoinjectors. This role

### Director, Clinical Operations - Oruka Therapeutics Inc
- Location: Waltham, Massachusetts, United States (unspecified)
- Salary: $213K-$240K
- Posted: 2026-05-29
- Apply: https://job-boards.greenhouse.io/oruka/jobs/5236048008
- Excerpt: Director, Clinical Operations Waltham, Massachusetts, United States About Us: Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture. Job Title: Director, Clinical Operations Location: Waltham, MA Hybrid - onsite 3 days/week required Reports To : Vice President, Clinical Operations Role Overview: We are seeking an exceptionally nimble and flexible Director of Clinical Operations who has a track record of achievement across all aspects of trial setup and execution in a fast paced small biotech with limited infrastructure and resources. The individual will successfully lead and optimize activity across multiple studies for Oruka Therapeutics. This critical role demands a strategic leader who possesses a keen ability to "zoom in" on intricate operational details

### Associate Director / Director, Device Development (Prefilled Syringes & Auto-Injectors) - Oruka Therapeutics Inc
- Location: Remote; Waltham, Massachusetts, United States (remote)
- Salary: $182K-$240K
- Posted: 2026-04-10
- Hires in: MA
- Apply: https://job-boards.greenhouse.io/oruka/jobs/5184889008
- Excerpt: Associate Director / Director, Device Development (Prefilled Syringes & Auto-Injectors) Remote; Waltham, Massachusetts, United States About Us: Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture. Job Title: Associate Director / Director, Device Development (Prefilled Syringes & Auto-Injectors) Location: Hybrid - Waltham, MA . Candidates will be required to be in-office 3 days/week. Remote may be considered. Position Summary We are seeking an experienced and driven Associate Director or Director of Device Development to lead the end-to-end development of drug delivery systems, with a focus on prefilled syringes and auto-injectors for late-stage programs and commercialization. This role will be responsible for integrating medical device engineering, human-centered design, and human factors engineering into

### Director, Analytical Development and Validation, Tech Ops (Biologics) - Oruka Therapeutics Inc
- Location: Remote; Waltham, Massachusetts, United States (remote)
- Salary: $213K-$240K
- Posted: 2026-04-10
- Hires in: MA
- Apply: https://job-boards.greenhouse.io/oruka/jobs/5184631008
- Excerpt: Director, Analytical Development and Validation, Tech Ops (Biologics) Remote; Waltham, Massachusetts, United States About Us: Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture. Job Title: Director, Analytical Development and Validation, Tech Ops (Biologics) Location: Hybrid - Waltham, MA . Candidates will be required to be in-office 3 days/week. Remote may be considered. Role Overview: The Director of Analytical Development and Validation will provide scientific and strategic leadership for late-stage analytical activities supporting the development, validation, and lifecycle management of biologic drug products, with a focus on monoclonal antibodies. This role will lead method validation and comparability efforts in support of BLA/MAA submissions, process changes, and commercial readiness, while partnering closely with

### Senior Manager/Associate Director Clinical Monitoring Strategy & Optimization - Oruka Therapeutics Inc
- Location: Menlo Park, California, United States; Remote; Waltham, Massachusetts, United States (remote)
- Salary: $161K-$208K
- Posted: 2026-06-06
- Apply: https://job-boards.greenhouse.io/oruka/jobs/5250171008
- Excerpt: Senior Manager/Associate Director Clinical Monitoring Strategy & Optimization Menlo Park, California, United States; Remote; Waltham, Massachusetts, United States About Us: Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture. Job Title: Sr. Manager/Associate Director, Clinical Monitoring Strategy and Optimization Location: Remote OR Hybrid 3 days/week if located near office in either Waltham, MA or Menlo Park, CA will be required. Role Overview: We are seeking an experienced and highly motivated Sr. Manager/Associate Director of Clinical Monitoring Strategy and Optimization to provide strategic and operational leadership for clinical monitoring activities across our development programs. This individual will play a critical role in building and scaling clinical operations infrastructure within a fast-paced emerging biotech

### Manager/Sr. Manager QA Supply Chain - Oruka Therapeutics Inc
- Location: Waltham, Massachusetts, United States (unspecified)
- Salary: $146K-$187K
- Posted: 2026-05-28
- Apply: https://job-boards.greenhouse.io/oruka/jobs/5234862008
- Excerpt: Manager/Sr. Manager QA Supply Chain Waltham, Massachusetts, United States About Us: Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture. Job Title: Manager / Senior Manager, QA Supply Chain Location: Hybrid - Waltham, MA . Candidates will be required to be in-office 3 days/week. Role Overview: The Manager / Senior Manager, QA Supply Chain is responsible for providing quality oversight of clinical supply chain activities supporting Phase 2 and Phase 3 programs, including packaging, labeling, distribution, and cold chain management. This role ensures inspection readiness and compliance across all clinical supply operations. This role ensures that all supply chain operations are conducted in compliance with cGMP, GCP, and GDP requirements, with a

### Principal or Associate Scientist, Analytical Development Japan (Late Stage), Pharmaceutical Sciences - Takeda Pharmaceutical Company Limited
- Location: Fujisawa, Japan (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-12
- 401(k) match: listed (not source-backed)
- Apply: https://takeda.wd3.myworkdayjobs.com/External/job/Fujisawa-Japan/Principal-or-Associate-Scientist--Analytical-Development-Japan--Late-Stage---Pharmaceutical-Sciences_R0181177-1
- Excerpt: Principal or Associate Scientist, Analytical Development Japan (Late Stage), Pharmaceutical Sciences Fujisawa, Japan posted: Posted Today

### Medical Science Liaison-Southeast - Oruka Therapeutics Inc
- Location: Remote (remote)
- Salary: $182K-$235K
- Posted: 2026-05-06
- Apply: https://job-boards.greenhouse.io/oruka/jobs/5212447008
- Excerpt: Medical Science Liaison-Southeast Remote About Us: Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture. Job Title: Medical Science Liaison- Southeast Location: Field-based, covering VA, WV, NC, SC, GA, FL, TN. The candidate is required to live in the territory. Role Overview: Oruka is looking for a Medical Science Liaison's (MSL), a field based scientific expert that strategically supports medical affairs objectives and serves as a conduit of communication between clinical community and Oruka's internal team. The MSL is responsible for developing and managing peer-to-peer relationships with a variety of health care professionals and engaging in high quality communications about Oruka's products and clinical trials in their territory. There is a special

### Lead Director, Pharmaceutical Contracting - CVS Health Corporation
- Location: Work at Home, Illinois, United States (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-10
- Non-birth-parent leave: 4 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://cvshealth.wd1.myworkdayjobs.com/CVS_Health_Careers/job/IL---Downers-Grove/Lead-Director--Pharmaceutical-Contracting_R0933942/apply
- Excerpt: Lead Director, Pharmaceutical Contracting Work at Home, Illinois, United States Join us as Lead Director, Pharmaceutical Contracting and drive high-impact negotiations with major pharmaceutical manufacturers. Shape strategy, foster partnerships, and lead rebate initiatives in a dynamic healthcare environment. If you excel in complex contract negotiations and thrive in leadership roles, this is your opportunity to make a significant impact.

### Sr. Outsourcing Associate, Clinical Outsourcing - Oruka Therapeutics Inc
- Location: Menlo Park, California, United States; Remote; Waltham, Massachusetts, United States (remote)
- Salary: $130K-$146K
- Posted: 2026-06-11
- Apply: https://job-boards.greenhouse.io/oruka/jobs/5255603008
- Excerpt: Sr. Outsourcing Associate, Clinical Outsourcing Menlo Park, California, United States; Remote; Waltham, Massachusetts, United States About Us: Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture. Job Title: Sr. Outsourcing Associate, Clinical Outsourcing Location: Remote or Hybrid 3 days/week if located near office in W altham, MA or Menlo Park, CA will be required. Role Overview The Sr. Outsourcing Associate, Clinical Outsourcing is responsible for supporting business aspects of vendor and site agreements across defined clinical service providers and other outsourcing needs for current and future clinical trials. Responsibilities include contract negotiations, budget management, contract quality control through the support the Clinical Operations, Biometrics and Medical Affairs departments in the oversight of

### Technician, Pharmaceutical - 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 (not source-backed)
- Apply: https://jobs.smartrecruiters.com/AbbVie/3743990013577016-technician-pharmaceutical
- Excerpt: Technician, Pharmaceutical 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: We are recruiting a Pharmaceutical Technician to join our team on site in Manorhamilton Road, Sligo on a 12 month fixed-term contract. This role is rotational shift work. In your role as Pharmaceutical Technician you will be responsible for producing drug product materials as per organizational needs in line with all relevant compliance requirements. This person will operate as a team member in a pharmaceutical processing facility in line with all regulatory and organizational requirements. A snapshot of your key responsibilities as a Pharmaceutical Technician would be: Pharmaceutical processing activities in our manufacturing building and support locations. Team co-ordination to maximise the effectiveness of the team members. Documentation of all activities in line with cGMP requirements. Cross training within the team and training of new team members. Participation in continuous improvement programs to implement improvements in the quality, safety, environmental and production systems. Execution of commissioning and validation protocols on an ongoing basis. Maintaining the overall cGMP of the pharmaceutical processing areas. Adheres

### Sr. Manager/Associate Director, Regulatory Affairs - Oruka Therapeutics Inc
- Location: Menlo Park, California, United States; Remote; Waltham, Massachusetts, United States (remote)
- Salary: $161K-$208K
- Posted: 2026-06-06
- Apply: https://job-boards.greenhouse.io/oruka/jobs/5250377008
- Excerpt: Sr. Manager/Associate Director, Regulatory Affairs Menlo Park, California, United States; Remote; Waltham, Massachusetts, United States About Us: Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture. Job Title: Sr. Manager/Associate Director, Regulatory Affairs Location : Preferred: Hybrid 3 days/week in office (Menlo Park, CA or Waltham, MA). Remote will be considered. Position Summary The Senior Manager / Associate Director, Regulatory Affairs will support regulatory activities for one or more development programs and contribute to the development and execution of global regulatory plans that support the advancement of Oruka's biologics portfolio. This individual will work closely with cross-functional teams to provide regulatory guidance throughout product development, support health authority interactions, and help ensure

### Senior Research Associate/Senior Scientist, Pharmaceutical Development - Ionis Pharmaceuticals
- Location: 2280 Faraday-USA; 2830 Whiptail (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-05
- 401(k) match: listed (not source-backed)
- Apply: https://recruiting.ultipro.com/isi1000isis/JobBoard/14a66400-68fa-4847-8593-af776328cfd2/OpportunityDetail?opportunityId=ad2d13f5-0499-4011-b6d6-e4be422f0485
- Excerpt: Senior Research Associate/Senior Scientist, Pharmaceutical Development 2280 Faraday-USA; 2830 Whiptail Ionis Pharmaceuticals seeks an experienced pharmaceutical development scientist to support laboratory experiments, review development data, and author and standardize technical reports for injectable drug products in development. The ideal candidate will be an independent self-starter with experience in analytical, formulation and process support for early and late-stage development of oligonucleotide-based drug products including conjugated with small molecules, peptides and proteins. The successful candidate will be able to perform the following responsibilities with a high degree of independence and attention to detail.

### Senior Paralegal/Senior Contracts Manager - Oruka Therapeutics Inc
- Location: Menlo Park, California, United States (unspecified)
- Salary: $161K-$187K
- Posted: 2026-05-22
- Apply: https://job-boards.greenhouse.io/oruka/jobs/5229654008
- Excerpt: Senior Paralegal/Senior Contracts Manager Menlo Park, California, United States About Us: Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture. Job Title: Senior Paralegal/Senior Contracts Manager Location: Hybrid - Menlo Park, CA. Onsite 3 days/week Role Overview: Our Senior Paralegal/Senior Contracts Manager will play a key role in managing day-to-day contracts and supporting a wide range of legal matters for a growing public biopharma company. This position is ideal for a proactive, highly organized professional who thrives in a fast-paced, collaborative environment. The ideal candidate will bring experience supporting small to mid-size legal departments, preferably within the life sciences industry, and be comfortable working across multiple projects with minimal supervision. Key Responsibilities:

### Senior Legal Counsel - Pharmaceutical Contracting - CVS Health Corporation
- Location: One CVS Drive, Woonsocket, Rhode Island,United States (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-26
- Non-birth-parent leave: 4 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://cvshealth.wd1.myworkdayjobs.com/CVS_Health_Careers/job/RI---Woonsocket/Senior-Legal-Counsel---Pharmaceutical-Contracting_R0901888/apply
- Excerpt: Senior Legal Counsel - Pharmaceutical Contracting One CVS Drive, Woonsocket, Rhode Island,United States Join our team as a Senior Legal Counsel - Pharmaceutical Contracting and play a pivotal role in shaping healthcare solutions. Advise on complex retail trade and pharmaceutical agreements, ensure regulatory compliance, and collaborate with cross-functional teams. Make a meaningful impact in a dynamic environment dedicated to innovation and patient care.

### Director of Biostatistics - Oruka Therapeutics Inc
- Location: Remote (remote)
- Salary: $213K-$240K
- Posted: 2026-05-20
- Apply: https://job-boards.greenhouse.io/oruka/jobs/5210738008
- Excerpt: Director of Biostatistics Remote About Us: Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture. Job Title: Director of Biostatistics Location: Remote OR Hybrid 3 days/week if located near office in either Waltham, MA or Menlo Park, CA will be required. Role Overview: The Director of Biostatistics will provide statistical leadership and strategic direction for our clinical development programs. This individual will serve as the lead biostatistician and will be responsible for providing expert guidance on study design, statistical analysis plans, and the interpretation of clinical trial results as well as statistical support for regulatory submission activities. The candidate will represent the Biostatistics function at internal and external meetings. The ideal candidate

### Pharmaceutical Assistant - Pfizer
- Location: United States - Kansas - McPherson (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 (not source-backed)
- Apply: https://pfizer.wd1.myworkdayjobs.com/PfizerCareers/job/United-States---Kansas---McPherson/Pharmaceutical-Assistant_4954329-1
- Excerpt: Pharmaceutical Assistant United States - Kansas - McPherson posted: Posted Today

### Medical Science Liaison-North Central - Oruka Therapeutics Inc
- Location: Remote (remote)
- Salary: $182K-$235K
- Posted: 2026-05-06
- Apply: https://job-boards.greenhouse.io/oruka/jobs/5212486008
- Excerpt: Medical Science Liaison-North Central Remote About Us: Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture. Job Title: Medical Science Liaison- North Central Location: Field-based, covering IL, IN, MI, WI, MO, OH, Western PA/Pittsburgh . The candidate is required to live in the territory. Role Overview: Oruka is looking for a Medical Science Liaison's (MSL), a field based scientific expert that strategically supports medical affairs objectives and serves as a conduit of communication between clinical community and Oruka's internal team. The MSL is responsible for developing and managing peer-to-peer relationships with a variety of health care professionals and engaging in high quality communications about Oruka's products and clinical trials in their territory.

### Pharmaceutical Attendant - Pfizer
- Location: United States - Kansas - McPherson (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-11
- Parental leave: 12 weeks (not source-backed)
- Non-birth-parent leave: 12 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://pfizer.wd1.myworkdayjobs.com/PfizerCareers/job/United-States---Kansas---McPherson/Pharmaceutical-Attendant_4956657-1
- Excerpt: Pharmaceutical Attendant United States - Kansas - McPherson posted: Posted Yesterday

### Medical Science Liaison-South Central - Oruka Therapeutics Inc
- Location: Remote (remote)
- Salary: $182K-$235K
- Posted: 2026-05-06
- Apply: https://job-boards.greenhouse.io/oruka/jobs/5212478008
- Excerpt: Medical Science Liaison-South Central Remote About Us: Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture. Job Title: Medical Science Liaison- South Central Location: Field-based, covering MS, LA, AR, OK, TX, AL, KS . The candidate is required to live in the territory. Role Overview: Oruka is looking for a Medical Science Liaison's (MSL), a field based scientific expert that strategically supports medical affairs objectives and serves as a conduit of communication between clinical community and Oruka's internal team. The MSL is responsible for developing and managing peer-to-peer relationships with a variety of health care professionals and engaging in high quality communications about Oruka's products and clinical trials in their territory. There

### Pharmaceutical Process Expert (PPE) - Ipsen
- Location: Wrexham (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- 401(k) match: listed (not source-backed)
- Apply: https://ipsen.wd103.myworkdayjobs.com/Ipsen_Careers/job/Wrexham/Pharmaceutical-Process-Expert--PPE-_R-21479
- Excerpt: Pharmaceutical Process Expert (PPE) Wrexham posted: Posted 30+ Days Ago

### Senior Scientific Communications Manager - Oruka Therapeutics Inc
- Location: Menlo Park, California, United States; Remote; Waltham, Massachusetts, United States (remote)
- Salary: $161K-$187K
- Posted: 2026-04-27
- Apply: https://job-boards.greenhouse.io/oruka/jobs/5202407008
- Excerpt: Senior Scientific Communications Manager Menlo Park, California, United States; Remote; Waltham, Massachusetts, United States About Us: Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture. Job Title: Senior Scientific Communications Manager Location: Remote OR Hybrid 3 days/week if located near office in either Waltham, MA or Menlo Park, CA will be required Role Overview: We're looking for a Senior Scientific Communications Manager to join our growing biotech team. This is a hands-on role for someone who enjoys turning complex scientific and clinical information into clear, accurate, and useful communications for a variety of audiences. At a small startup, this person will wear multiple hats. You'll help shape our scientific story externally and

### Account Manager - Pharmaceutical - Amcor
- Location: 16 Locations (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- 401(k) match: listed (not source-backed)
- Apply: https://amcor.wd5.myworkdayjobs.com/Amcor_External_Career_Site/job/AF-Deerfield-IL-Corporate/Account-Manager---Pharmaceutical_REQ_89081
- Excerpt: Account Manager - Pharmaceutical 16 Locations posted: Posted 30+ Days Ago

### Medical Science Liaison-Northeast - Oruka Therapeutics Inc
- Location: Remote (remote)
- Salary: $182K-$235K
- Posted: 2026-05-06
- Apply: https://job-boards.greenhouse.io/oruka/jobs/5212107008
- Excerpt: Medical Science Liaison-Northeast Remote About Us: Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture. Job Title: Medical Science Liaison- Northeast Location: Field-based, covering MA, ME, NH, VT, CT, RI, NY, NJ, MD/DC, Eastern PA . The candidate is required to live in the territory. Role Overview: Oruka is looking for a Medical Science Liaison's (MSL), a field based scientific expert that strategically supports medical affairs objectives and serves as a conduit of communication between clinical community and Oruka's internal team. The MSL is responsible for developing and managing peer-to-peer relationships with a variety of health care professionals and engaging in high quality communications about Oruka's products and clinical trials in their

### M23 Pharmaceutical Attendant - Pfizer
- Location: United States - Kansas - McPherson (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-11
- Parental leave: 12 weeks (not source-backed)
- Non-birth-parent leave: 12 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://pfizer.wd1.myworkdayjobs.com/PfizerCareers/job/United-States---Kansas---McPherson/M23-Pharmaceutical-Attendant_4956770-2
- Excerpt: M23 Pharmaceutical Attendant United States - Kansas - McPherson posted: Posted Yesterday

### Scientist, Downstream, Process Development and Manufacturing (PD/MFG) (Biologics) - Oruka Therapeutics Inc
- Location: Waltham, Massachusetts, United States (unspecified)
- Salary: $130K-$146K
- Posted: 2026-05-27
- Apply: https://job-boards.greenhouse.io/oruka/jobs/5232207008
- Excerpt: Scientist, Downstream, Process Development and Manufacturing (PD/MFG) (Biologics) Waltham, Massachusetts, United States About Us: Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture. Job Title: Scientist, Downstream, Process Development and Manufacturing (PD/MFG) (Biologics) Location: Hybrid - Waltham, MA . Candidates will be required to be in-office 3 days/week. Role Overview: We are seeking a motivated Process Development individual to lead downstream pre-clinical to early stage enabling process development, optimization, scale-up and transfer of manufacturing activities. In this role, the ideal candidate will be responsible for early-stage process development, tox batch production, optimization, scale up to GMP and late stage pivotal development. The successful candidate will be involved in pre-clinical development to pre-pivotal

### Senior Analyst - Pharmaceutical Markets - IQVIA
- Location: Madrid, Spain (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- 401(k) match: listed (not source-backed)
- Apply: https://iqvia.wd1.myworkdayjobs.com/IQVIA/job/Madrid-Spain/Senior-Analyst---Pharmaceutical-Markets_R1537065
- Excerpt: Senior Analyst - Pharmaceutical Markets Madrid, Spain posted: Posted 30+ Days Ago

### Director, Clinical Quality Assurance - Oruka Therapeutics Inc
- Location: Waltham, Massachusetts, United States (unspecified)
- Salary: $213K-$240K
- Posted: 2026-04-09
- Apply: https://job-boards.greenhouse.io/oruka/jobs/5182408008
- Excerpt: Director, Clinical Quality Assurance Waltham, Massachusetts, United States About Us: Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture. Job Title: Director, Clinical Quality Assurance Location: Remote; Waltham, MA area candidates preferred. Role Overview: The Director, Clinical Quality Assurance is responsible for providing strategic quality leadership, support, and oversight for Oruka's clinical development activities, with primary focus on Good Clinical Practice (GCP) and related quality systems supporting clinical trials. This role will establish, improve, and lead phase-appropriate clinical quality processes, ensure robust oversight of clinical trial execution and vendor performance, and drive inspection readiness for global health authority inspections, including FDA Bioresearch Monitoring (BIMO) inspections. This role will partner closely with Clinical

### Pharmaceutical Cleaner - AstraZeneca
- Location: Australia – New South Wales (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-03
- 401(k) match: listed (not source-backed)
- Apply: https://astrazeneca.wd3.myworkdayjobs.com/Careers/job/Australia--New-South-Wales/Pharmaceutical-Cleaner_R-251307
- Excerpt: Pharmaceutical Cleaner Australia – New South Wales posted: Posted 9 Days Ago

### Scientist/Senior Scientist, Upstream, Process Development & Manufacturing (Biologics) - Oruka Therapeutics Inc
- Location: Remote; Waltham, Massachusetts, United States (remote)
- Salary: $130K-$208K
- Posted: 2026-04-17
- Hires in: MA
- Apply: https://job-boards.greenhouse.io/oruka/jobs/5192663008
- Excerpt: Scientist/Senior Scientist, Upstream, Process Development & Manufacturing (Biologics) Remote; Waltham, Massachusetts, United States About Us: Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture. Job Title: Scientist / Senior Scientist, Upstream, Process Development & Manufacturing (Biologics) Location: Hybrid - Waltham, MA required to be in-office 3 days/week -OR- Remote Position Overview: We are seeking an experienced and motivated Scientist/Senior Scientist to support upstream manufacturing activities. This role will be instrumental in contributing to process development and delivery of clinical trial material at CDMOs. The ideal candidate will collaborate cross-functionally within the CMC team including downstream, analytical, and drug product and other stakeholders such as QA, regulatory, and program management. The successful candidate

### Pharmaceutical representative - The Procter & Gamble Company
- Location: BUDAPEST GO - LIBERTY (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-19
- Parental leave: 8 weeks (not source-backed)
- Non-birth-parent leave: 8 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://pg.wd5.myworkdayjobs.com/1000/job/BUDAPEST-GO---LIBERTY/Pharmaceutical-representative_R000151450
- Excerpt: Pharmaceutical representative BUDAPEST GO - LIBERTY posted: Posted 24 Days Ago

### Accounting Manager - Oruka Therapeutics Inc
- Location: Menlo Park, California, United States (unspecified)
- Salary: $146K-$161K
- Posted: 2026-05-28
- Apply: https://job-boards.greenhouse.io/oruka/jobs/5234891008
- Excerpt: Accounting Manager Menlo Park, California, United States About Us: Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture. Job Title: Accounting Manager Location: Menlo Park, CA. Hybrid - onsite 3 days/week is required. Reports To : Sr. Director, Controller We are looking for a motivated and knowledgeable Accounting Manager to play a key role in accounting at a fast-paced public biotech company. Reporting to the Sr. Director, Controller, the Accounting Manager will be responsible for clinical trial accounting accruals and other accruals and prepaids. The ideal candidate will have a strong understanding of accruals of clinical trial costs in biotech industry, excellent analytical skills, and the ability to work effectively in a

### Graphic Designer – Pharmaceutical Marketing - Amgen
- Location: India - Hyderabad (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- Parental leave: 6 weeks (not source-backed)
- Non-birth-parent leave: 6 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://amgen.wd1.myworkdayjobs.com/Careers/job/India---Hyderabad/Graphic-Designer---Pharmaceutical-Marketing_R-240424
- Excerpt: Graphic Designer – Pharmaceutical Marketing India - Hyderabad posted: Posted 30+ Days Ago

### Biosample Operations Associate/Sr. Associate - Oruka Therapeutics Inc
- Location: Menlo Park, California, United States; Remote; Waltham, Massachusetts, United States (remote)
- Salary: $104K-$146K
- Posted: 2026-06-11
- Apply: https://job-boards.greenhouse.io/oruka/jobs/5255863008
- Excerpt: Biosample Operations Associate/Sr. Associate Menlo Park, California, United States; Remote; Waltham, Massachusetts, United States About Us: Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture. Job Title: Biosample Operations Associate/Senior Associate Location: Remote or Hybrid 3 days/week if located near office in W altham, MA or Menlo Park, CA will be required. Role Overview: The Biosample Operations Associate/Senior Associate is responsible for supporting the operational management of clinical trial biospecimens throughout the sample lifecycle. This role serves as the primary liaison between investigative sites, central laboratories, specialty testing laboratories, clinical operations, and study vendors to ensure the accurate tracking, transfer, reconciliation, and documentation of clinical trial samples. The Biosample Operations Associate/Senior Associate

### Pharmaceutical CIP/COP Technical Coordinator - Ecolab
- Location: 3 Locations (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-19
- Parental leave: 6 weeks (not source-backed)
- Non-birth-parent leave: 6 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://ecolab.wd1.myworkdayjobs.com/Ecolab_External/job/DEU---Nordrhein-Westfalen---Monheim-am-Rhein/Pharmaceutical-CIP-COP-Technical-Coordinator_R00291546
- Excerpt: Pharmaceutical CIP/COP Technical Coordinator 3 Locations posted: Posted 24 Days Ago

### Clinical Trial Manager/Senior Clinical Trial Manager - Oruka Therapeutics Inc
- Location: Waltham, Massachusetts, United States (unspecified)
- Salary: $146K-$187K
- Posted: 2026-04-10
- Apply: https://job-boards.greenhouse.io/oruka/jobs/5184329008
- Excerpt: Clinical Trial Manager/Senior Clinical Trial Manager Waltham, Massachusetts, United States About Us: Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture. Job Title: Clinical Trial Manager/Senior Clinical Trial Manager Location: Hybrid 3 days/week if located near office in Waltham, MA or Menlo Park, CA will be required. Remote may be considered. About Us: Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per

### Pharmaceutical Strategic Account Manager - Becton Dickinson
- Location: 2 Locations (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-08
- 401(k) match: listed (not source-backed)
- Apply: https://bdx.wd1.myworkdayjobs.com/EXTERNAL_CAREER_SITE_USA/job/USA---Massachusetts---Boston/Pharmaceutical-Strategic-Account-Manager_R-547506-1
- Excerpt: Pharmaceutical Strategic Account Manager 2 Locations posted: Posted 4 Days Ago

### Director, GMP Quality Assurance - Oruka Therapeutics Inc
- Location: Menlo Park, California, United States; Remote; Waltham, Massachusetts, United States (remote)
- Salary: $213K-$240K
- Posted: 2026-05-28
- Apply: https://job-boards.greenhouse.io/oruka/jobs/5234842008
- Excerpt: Director, GMP Quality Assurance Menlo Park, California, United States; Remote; Waltham, Massachusetts, United States About Us: Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture. Job Title: Director, GMP Quality Assurance Location: Hybrid - Waltham, MA or Menlo Park, CA. Candidates will be required to be in-office 3 days/week. Open to remote for non-local candidates. Role Overview: The Director of GMP Quality Assurance, reporting to the Senior Director of GMP Quality, will be responsible for providing quality oversight for Oruka's clinical development programs and manufacturing. You will be responsible to ensure Oruka's programs are advanced through the development pipeline in compliance with phase-appropriate regulatory requirements, applicable guidelines, and industry best practices. You

### Pharmaceutical Production Lead - All Shifts - Medline Inc.
- Location: Waukegan, Illinois (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-14
- 401(k) match: listed (not source-backed)
- Apply: https://medline.wd5.myworkdayjobs.com/Medline/job/Waukegan-Illinois/Pharmaceutical-Production-Lead---All-Shifts_R2605412
- Excerpt: Pharmaceutical Production Lead - All Shifts Waukegan, Illinois posted: Posted 29 Days Ago

### Early Development Team Leader - Arvinas Inc
- Location: Remote, Hybrid, New Haven - CT (hybrid)
- Salary: Not disclosed
- Posted: 2026-04-01
- Hires in: CT
- Apply: https://job-boards.greenhouse.io/arvinas/jobs/7686687003
- Excerpt: Early Development Team Leader Remote, Hybrid, New Haven - CT Arvinas is a clinical-stage biotechnology company dedicated to improving the lives of patients suffering from debilitating and life-threatening diseases through the discovery, development, and commercialization of therapies that degrade disease-causing proteins. Arvinas uses its proprietary PROTAC Discovery Engine platform to engineer proteolysis targeting chimeras, or PROTAC targeted protein degraders, that are designed to harness the body's own natural protein disposal system to selectively and efficiently degrade and remove disease-causing proteins. In addition to its robust preclinical pipeline of PROTAC protein degraders against validated and “undruggable” targets, the company has three investigational clinical-stage programs currently enrolling: ARV-102 for the treatment of patients with neurodegenerative disorders,ARV-393 for the treatment of patients with relapsed/refractory non-Hodgkin Lymphoma and potentially other lymphomas, and ARV-806, a KRAS G12D PROTAC for the treatment patients with solid tumors with KRAS G12D mutations. On August 8 th 2025, the U.S. Food and Drug Administration (FDA) accepted the New Drug Application (NDA) for vepdegestrant- an investigational, orally bioavailable PROTAC estrogen receptor degrader- for its use as a monotherapy in the treatment of adults with estrogen receptor-positive (ER+), human epidermal growth factor receptor 2-negative (HER2-), ESR1-mutated advanced or metastatic breast cancer previously treated with endocrine-based therapy. In September 2025, Arvinas and Pfizer announced their plan to jointly select a third party for the out-licensing and commercialization of vepdegestrant. In April 2024, Arvinas entered into a transaction with Novartis, including a global license agreement for the development and commercialization of the clinical

### Pharmaceutical Manufacturer Relations Executive - Humana Inc.
- Location: Remote Nationwide (remote)
- Salary: Not disclosed
- Posted: 2026-06-10
- 401(k) match: listed (not source-backed)
- Apply: https://humana.wd5.myworkdayjobs.com/CenterWell_External_Career_Site/job/Remote-Nationwide/Pharmaceutical-Manufacturer-Relations-Executive_R-419074
- Excerpt: Pharmaceutical Manufacturer Relations Executive Remote Nationwide posted: Posted 2 Days Ago

### Administrative Assistant - Oruka Therapeutics Inc
- Location: Waltham, Massachusetts, United States (unspecified)
- Salary: $35-$50/hr
- Posted: 2026-06-11
- Apply: https://job-boards.greenhouse.io/oruka/jobs/5255845008
- Excerpt: Administrative Assistant Waltham, Massachusetts, United States About Us: Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture. Job Title: Administrative Assistant Location: Waltham, MA / Onsite presence 2-3 days per week required Role Overview: We are seeking a highly organized, proactive, and detail-oriented Administrative Assistant to support daily business operations and help maintain an efficient, collaborative work environment. The Administrative Assistant will provide administrative and operational support across multiple functions, including executive scheduling, office management, meeting coordination, vendor management, and general administrative activities. This role is ideal for someone who thrives in a fast-paced, mission-driven environment and enjoys supporting a dynamic team. Key Responsibilities Administrative Support - Proactively manage complex, multi-time-zone calendars

### Lead Director, Pharmaceutical Contracting - CVS Health Corporation
- Location: 4 Locations (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-10
- Parental leave: 4 weeks (not source-backed)
- Non-birth-parent leave: 4 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://cvshealth.wd1.myworkdayjobs.com/CVS_Health_Careers/job/IL---Downers-Grove/Lead-Director--Pharmaceutical-Contracting_R0933942
- Excerpt: Lead Director, Pharmaceutical Contracting 4 Locations posted: Posted 2 Days Ago

### Medical Science Liaison-Northwest - Oruka Therapeutics Inc
- Location: Remote (remote)
- Salary: $182K-$235K
- Posted: 2026-05-06
- Apply: https://job-boards.greenhouse.io/oruka/jobs/5212489008
- Excerpt: Medical Science Liaison-Northwest Remote About Us: Oruka Therapeutics (Nasdaq: ORKA) is developing novel biologics designed to set a new standard for the treatment of chronic skin diseases. Oruka's mission is to offer patients suffering from chronic skin diseases like plaque psoriasis the greatest possible freedom from their condition by achieving high rates of complete disease clearance with dosing as infrequently as once or twice per year. Oruka is advancing a proprietary portfolio of potentially best-in-class antibodies that were engineered by Paragon Therapeutics and target the core mechanisms underlying plaque psoriasis and other dermatologic and inflammatory diseases. For more information, visit www.orukatx.com As we build our core team, we're seeking top talent in different functional areas who are not just looking for a job, but an opportunity to be part of something bigger. Someone who is passionate about making a difference and eager to contribute to establishing an engaged, inclusive, and positive company culture. Job Title: Medical Science Liaison- Northwest Location: Field-based, covering CO, WY, UT, MT, ID, OR, WA, IA, ND, SD . The candidate is required to live in the territory. Role Overview: Oruka is looking for a Medical Science Liaison's (MSL), a field based scientific expert that strategically supports medical affairs objectives and serves as a conduit of communication between clinical community and Oruka's internal team. The MSL is responsible for developing and managing peer-to-peer relationships with a variety of health care professionals and engaging in high quality communications about Oruka's products and clinical trials in their territory.

### Assoc Director/Director, Pharmaceutical Development - Erasca Inc
- Location: South San Francisco, CA (unspecified)
- Salary: $200K-$225K
- Posted: 2026-06-11
- 401(k) match: listed (not source-backed)
- Mental health support: yes (not source-backed)
- Apply: https://job-boards.greenhouse.io/erasca/jobs/7769033003
- Excerpt: Assoc Director/Director, Pharmaceutical Development South San Francisco, CA Erasca is a clinical-stage precision oncology company focused on discovering, developing and commercializing medicines for the benefit of patients with cancer. Our programs take novel approaches to shutting down one of cancer's most commonly mutated signaling cascades, the RAS/MAPK pathway, which affects approximately 5.5 million lives each year worldwide. The name “Erasca” has an important embedded meaning: it is a contraction of our audacious hope to “erase cancer” that drives our mission and everything that we do on behalf of patients with cancer. Position Summary: Reporting to the Sr Director Pharmaceutical Development, the Associate Director or Director of Pharmaceutical Development will be a liaison for the manufacture of Erasca's small molecule development drug products (DPs) at external contract development and manufacturing organizations (CDMOs). This individual will work on cross functional teams with colleagues from process development, analytical, formulation development, supply chain, QA, and regulatory CMC to plan, coordinate, and execute internal and external DP development and manufacturing activities. Essential Duties and Responsibilities: - Provide scientific, technical, and strategic direction to the design, development, and manufacture of investigational drug products from pre-clinical/clinical to commercial stage. - Manage activities and contractual relationship with contract manufacturers and laboratories performing product/formulation development, manufacturing, analytical development and testing, stability, and validation services. - Lead and collaborate with cross functional project team members to meet CMC goals. - Represent CMC DP and provide strategic recommendations and status reporting to cross-functional program team. - Author, review, and/or approve development

### Pharmaceutical Internship - Pharmaziepraktikum* (f/m/d) - The Procter & Gamble Company
- Location: Schwalbach Am Taunus (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-18
- Parental leave: 8 weeks (not source-backed)
- Non-birth-parent leave: 8 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://pg.wd5.myworkdayjobs.com/1000/job/Schwalbach-Am-Taunus/Pharmaceutical-Internship----Pharmaziepraktikum---f-m-d-_R000151566
- Excerpt: Pharmaceutical Internship - Pharmaziepraktikum* (f/m/d) Schwalbach Am Taunus posted: Posted 25 Days Ago

### Pharmaceutical Product Operator - All Shifts - Medline Inc.
- Location: Waukegan, Illinois (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-14
- 401(k) match: listed (not source-backed)
- Apply: https://medline.wd5.myworkdayjobs.com/Medline/job/Waukegan-Illinois/Pharmaceutical-Product-Operator_R2605410
- Excerpt: Pharmaceutical Product Operator - All Shifts Waukegan, Illinois posted: Posted 29 Days Ago

### OIC Developer - Anduril
- Location: Costa Mesa, California, United States (unspecified)
- Salary: $129K-$171K
- Posted: 2026-02-20
- Apply: https://boards.greenhouse.io/andurilindustries/jobs/5058262007?gh_jid=5058262007
- Excerpt: OIC Developer Costa Mesa, California, United States Anduril Industries is a defense technology company with a mission to transform U.S. and allied military capabilities with advanced technology. By bringing the expertise, technology, and business model of the 21st century's most innovative companies to the defense industry, Anduril is changing how military systems are designed, built and sold. Anduril's family of systems is powered by Lattice OS, an AI-powered operating system that turns thousands of data streams into a realtime, 3D command and control center. As the world enters an era of strategic competition, Anduril is committed to bringing cutting-edge autonomy, AI, computer vision, sensor fusion, and networking technology to the military in months, not years. ABOUT THE JOB: We are looking for an expert Oracle Integration Developer to join our Arsenal (Enterprise Systems) team. Your immediate mission: take ownership of our critical enterprise integrations connecting Oracle Fusion ERP with our upstream and downstream systems. These integrations, built on Oracle Integration Cloud, form the digital backbone that governs how we manage our business operations, from product data and procurement to manufacturing and financial processes. You will be tasked with stabilizing, optimizing, and making them exceptionally robust. Long-term, you will be the subject matter expert responsible for architecting and scaling our enterprise integration landscape. This is a high-impact role for someone who thrives on solving complex data challenges and wants to build the operational foundation that enables Anduril to scale its mission. WHAT YOU"LL DO: - Stabilize & Optimize: Dive deep into

### Senior Director, Executive & Enterprise Communications - Revolution Medicines
- Location: Redwood City, California, United States (unspecified)
- Salary: $244K-$305K
- Posted: 2026-05-01
- 401(k) match: listed (not source-backed)
- Apply: https://www.revmed.com/careers-list/?gh_jid=7613269003
- Excerpt: Senior Director, Executive & Enterprise Communications Redwood City, California, United States Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company's R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway. The Opportunity: The Senior Director, Executive & Enterprise Communications will serve as a trusted communications advisor to the CEO and select senior leaders while leading enterprise internal communications across a growing global organization. This is a high-impact role for a communicator who can operate strategically and execute with excellence. Success in this position requires sound judgment, executive presence, strong writing skills, and the ability to move seamlessly between shaping a CEO keynote and building the communications infrastructure that keeps teams informed, aligned, and engaged. Reporting to the Head of Communications, this role partners closely with the Corporate Communications lead, the Associate Director of Internal Communications, and regional communications and HR partners globally. This is a rare opportunity to work directly with RevMed's executive leadership team, shaping executive voice, internal culture, and enterprise communications at a company rapidly building toward commercial stage. Key responsibilities

### Apprentice Chemical and Pharmaceutical Technologist 2026 - Biogen
- Location: Solothurn, Switzerland (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- 401(k) match: listed (not source-backed)
- Apply: https://biibhr.wd3.myworkdayjobs.com/external/job/Solothurn-Switzerland/Apprentice-Chemical-and-Pharmaceutical-Technologist-2026_REQ21851
- Excerpt: Apprentice Chemical and Pharmaceutical Technologist 2026 Solothurn, Switzerland posted: Posted 30+ Days Ago

### Patient Admissions Coordinator - Patient Access - Providence
- Location: Mission Hills, CA, United States (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-10
- 401(k) match: listed (not source-backed)
- Apply: https://evac.fa.us2.oraclecloud.com/hcmUI/CandidateExperience/en/sites/CX/requisitions/job/427888
- Excerpt: Patient Admissions Coordinator - Patient Access Mission Hills, CA, United States One Revenue Cycle (ORC) is the name adopted to reflect the Providence employees who work throughout Providence Health & Services (PH&S) in revenue cycle systems and structures in support of our ministries and operations in all regions from Alaska to California. ORC's objective is to ensure our core strategy, One Ministry Committed to Excellence, is delivered along with the enhanced overall patient care experience (know me, care for me, ease my way) by providing a robust foundation of services, operational and technical support, and the sharing of comprehensive, relevant, and highly specialized revenue cycle expertise.

### Pharmaceutical Production Technician - All Shifts - Medline Inc.
- Location: Waukegan, Illinois (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-14
- 401(k) match: listed (not source-backed)
- Apply: https://medline.wd5.myworkdayjobs.com/Medline/job/Waukegan-Illinois/Pharmaceutical-Production-Technician---All-Shifts_R2605411
- Excerpt: Pharmaceutical Production Technician - All Shifts Waukegan, Illinois posted: Posted 29 Days Ago

### Director, Product Management – Pharmacy - Oracle
- Location: United States, US (unspecified)
- Salary: $139K-$306K
- Posted: 2026-06-01
- Parental leave: 14 weeks (not source-backed)
- Non-birth-parent leave: 14 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Adoption assistance: yes (not source-backed)
- Apply: https://careers.oracle.com/en/sites/jobsearch/job/335152/
- Excerpt: Director, Product Management – Pharmacy United States, US Oracle Health is transforming the future of medication management through intelligent, connected, and AI-enabled solutions that improve patient safety, operational efficiency, and clinical outcomes. Our Pharmacy portfolio plays a critical role in connecting prescribing, verification, dispensing, administration, and medication intelligence across the healthcare ecosystem. We are seeking a visionary Director of Product Management to lead Oracle Health's Pharmacy portfolio and drive the next generation of Pharmacy Reimagine initiatives. This leader will define and execute the product strategy for a portfolio of pharmacy solutions while helping shape AI-enabled applications within the Oracle Health AI Application Suite. The ideal candidate combines deep pharmacy domain expertise with exceptional product leadership experience and a passion for solving complex healthcare challenges. They will work closely with customers, clinicians, engineers, designers, data scientists, and executive leaders to deliver innovative solutions that transform how pharmacy teams operate across inpatient, ambulatory, military, veteran, and emerging care settings. This is a highly visible leadership role responsible for balancing strategic innovation, customer needs, business growth, and operational excellence across a broad product portfolio. Define the Pharmacy Portfolio Vision and Strategy Establish and communicate a compelling long-term vision for Oracle Health's Pharmacy portfolio. Lead the Pharmacy portfolio strategy and roadmap, including identifying opportunities to modernize medication workflows through using automation, use of AI, intelligent decision support. Drive portfolio investment decisions aligned with current and new products, customer needs, market opportunities, regulatory requirements, and Oracle Health's strategic objectives. Partner with executive leadership to define

### Pharmaceutical Representative (Dnipro) - Abbott Laboratories
- Location: Ukraine > Kyiv: Senator Business Center (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-11
- Parental leave: 8 weeks (not source-backed)
- Non-birth-parent leave: 8 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://abbott.wd5.myworkdayjobs.com/abbottcareers/job/Ukraine--Kyiv-Senator-Business-Center/Pharmaceutical-Representative--Dnipro-_31153247
- Excerpt: Pharmaceutical Representative (Dnipro) Ukraine > Kyiv: Senator Business Center posted: Posted Yesterday

### Director, Patient Marketing - Crinetics Pharmaceuticals INC
- Location: Remote (remote)
- Salary: $193K-$241K
- Posted: 2026-06-06
- 401(k) match: listed (not source-backed)
- Apply: https://crinetics.wd12.myworkdayjobs.com/CrineticsCareers/job/Remote/Director--Patient-Engagement_JR000495
- Excerpt: Director, Patient Marketing Remote Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. We are driven by science with a patient-centric and team-oriented culture. Crinetics is known for its inclusive workplace culture. We are also a dog-friendly workplace. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully integrated endocrine company from discovery to patients. Join our team as we transform the lives of others. Position Summary: The Director, Patient Marketing, will be instrumental in crafting and implementing strategies and tactics tailored to the rare disease community. Your responsibilities will include spearheading a range of initiatives, from near-term execution to developing new capabilities for mid-to-long-term brand success. This encompasses managing educational initiatives, cultivating relationships with key opinion leaders, and ensuring all marketing initiatives for patients and healthcare professionals adhere to company compliance standards. Essential Job Functions and Responsibilities: These may include but are not limited to: Develop comprehensive patient-centric strategies across multiple disease states including understanding the patient journey, identifying unmet needs, developing innovative solutions, and executing programs to meet those needs. Lead patient ambassador programs to include

### Demand Planner - Novartis
- Location: Bogota (Pharmaceuticals / GDD / NTO / CTS) (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-18
- 401(k) match: listed (not source-backed)
- Apply: https://novartis.wd3.myworkdayjobs.com/Internal_Careers_for_Acquired_Entities/job/Bogota-Pharmaceuticals--GDD--NTO--CTS/Demand-Planner_REQ-10078093
- Excerpt: Demand Planner Bogota (Pharmaceuticals / GDD / NTO / CTS) posted: Posted 25 Days Ago

### Executive Director, AI/ML Drug Discovery Analytics - Revolution Medicines
- Location: Redwood City, California, United States (unspecified)
- Salary: $326K-$383K
- Posted: 2026-04-10
- 401(k) match: listed (not source-backed)
- Apply: https://www.revmed.com/careers-list/?gh_jid=7695158003
- Excerpt: Executive Director, AI/ML Drug Discovery Analytics Redwood City, California, United States Revolution Medicines is a late-stage clinical oncology company developing novel targeted therapies for patients with RAS-addicted cancers. The company's R&D pipeline comprises RAS(ON) inhibitors designed to suppress diverse oncogenic variants of RAS proteins. The company's RAS(ON) inhibitors daraxonrasib (RMC-6236), a RAS(ON) multi-selective inhibitor; elironrasib (RMC-6291), a RAS(ON) G12C-selective inhibitor; zoldonrasib (RMC-9805), a RAS(ON) G12D-selective inhibitor; and RMC-5127, a RAS(ON) G12V-selective inhibitor, are currently in clinical development. As a new member of the Revolution Medicines team, you will join other outstanding professionals in a tireless commitment to patients with cancers harboring mutations in the RAS signaling pathway. The Opportunity: As Executive Director, AI/ML Drug Discovery Analytics, you will be a senior leader shaping the future of data-driven drug discovery at Revolution Medicines. You will define the Research's AI/ML strategy, oversee implementation of advanced analytics across discovery and build a world-class team to unlock the full potential of our rich internal datasets and make these insights accessible to other scientist. Your leadership will directly influence early discovery innovation, pipeline acceleration, and strategic portfolio decisions. Responsibilities include: Technical Leadership and Innovation: You will have a deep understanding of Machine Learning Operations and AI system design. Design and scale a robust ML infrastructure, integrating MLOps best practices to ensure seamless development, deployment, and monitoring of AI/ML models. Drive innovation in applying deep learning, generative models, and diffusion models to drug discovery, including target prediction, hit identification, and lead optimization. Leverage RevMed's unique datasets

### Commercial Excellence Manager (Pharmaceutical / Lifesciences) - IQVIA
- Location: Leiden, Netherlands (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-04
- 401(k) match: listed (not source-backed)
- Apply: https://iqvia.wd1.myworkdayjobs.com/IQVIA/job/Leiden-Netherlands/Commercial-Excellence-Manager--Pharmaceutical---Lifesciences-_R1549255
- Excerpt: Commercial Excellence Manager (Pharmaceutical / Lifesciences) Leiden, Netherlands posted: Posted 8 Days Ago

### Senior Vice President, Sales - Amylyx Pharmaceuticals Inc
- Location: Flexible/ U.S. Based (unspecified)
- Salary: $353K-$397K
- Posted: 2026-05-13
- 401(k) match: listed (not source-backed)
- Apply: https://job-boards.greenhouse.io/amylyx/jobs/5994725004
- Excerpt: Senior Vice President, Sales Flexible/ U.S. Based Amylyx has an audacious mission to usher in a new era for treating diseases with high unmet needs. Where others see challenges, we see opportunities that we pursue with urgency, rigorous science, and unwavering commitment to the communities we serve. We are a clinical-stage company currently focused on post-bariatric hypoglycemia (PBH), Wolfram syndrome, and amyotrophic lateral sclerosis (ALS). Our mission is powered by our people. Our core values - be audacious, be curious, be authentic, be engaged, and be accountable - creating a culture of caring. Amylyx has assembled an experienced team ready to take action because the communities we serve have no time to wait. If you share our passion and are determined to tackle some of medicine's toughest problems, we encourage you to read the opportunity below and apply. The Opportunity The SVP of Sales will play a critical leadership role in building and executing the commercial strategy for a pre‑commercial biotechnology company preparing for its first product launch. This individual will be responsible for designing and implementing the Go‑To‑Market (GTM) strategy, recruiting and developing a high‑performing sales organization, establishing strong relationships with Key Opinion Leaders (KOLs), ensuring full sales force readiness ahead of launch and driving performance. We anticipate hiring the Senior Vice President, Sales in September 2026. The ideal candidate combines strategic vision with hands‑on execution experience in specialty pharma or biotech launches and thrives in a fast‑paced, build‑from‑scratch environment. Responsibilities Enterprise Commercial Leadership - Shape overall U.S. commercial

### Manager, Pharmaceutical Sales Training - Asahi Kasei Corp.
- Location: Cary, NC (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- 401(k) match: listed (not source-backed)
- Apply: https://akamerica.wd501.myworkdayjobs.com/aka/job/Cary-NC/Manager--Pharmaceutical-Sales-Training_R5468-1
- Excerpt: Manager, Pharmaceutical Sales Training Cary, NC posted: Posted 30+ Days Ago

### Pharmaceutical QC Technical Services Manager - Smithfield Foods
- Location: Cincinnati, OH (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-22
- 401(k) match: listed (not source-backed)
- Apply: https://smithfieldfoods.wd1.myworkdayjobs.com/Careers/job/Cincinnati-OH/Pharmaceutical-QC-Technical-Services-Manager_R-2026-6094
- Excerpt: Pharmaceutical QC Technical Services Manager Cincinnati, OH posted: Posted 21 Days Ago

### SBM/BM-BC Dex-上海 - AstraZeneca
- Location: China (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- 401(k) match: listed (not source-backed)
- Apply: https://astrazeneca.wd3.myworkdayjobs.com/Careers/job/China/SBM-BM-BC-Dex-_R-251741
- Excerpt: SBM/BM-BC Dex-上海 China posted: Posted 30+ Days Ago

### Senior Director, Pharmaceutical Strategy and Development Leader - Crinetics Pharmaceuticals INC
- Location: San Diego, CA (unspecified)
- Salary: $214K-$268K
- Posted: 2026-05-12
- 401(k) match: listed (not source-backed)
- Apply: https://crinetics.wd12.myworkdayjobs.com/CrineticsCareers/job/San-Diego-CA/Senior-Director--Pharmaceutical-Strategy-and-Development-Leader_JR000446
- Excerpt: Senior Director, Pharmaceutical Strategy and Development Leader San Diego, CA Crinetics is a pharmaceutical company based in San Diego, California that develops much-needed therapies for people with rare endocrine diseases. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and robust pipeline across preclinical and clinical development. We are driven by science with a patient-centric and team-oriented culture. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully integrated endocrine company from discovery to patients. Come join our team as we transform the lives of others. Position Summary: The Senior Director, Pharmaceutical Development Team Leader (PDTL) is responsible for developing and leading the execution of comprehensive, compound-specific Technical Operations strategies to meet the global project team's (GPT) needs. This role provides leadership to interdisciplinary teams, managing multiple assets through various stages of development, and collaborates with various functional areas to achieve optimal development and business results. Essential Job Functions and Responsibilities: These may include but are not limited to: Develop, refine, update, and oversee Technical Operations project plans from multiple inputs, with emphasis on the alignment of these plans with strategic objectives, the decomposition of major objectives into discrete WBS-level work packages, the mapping of internal and cross-functional interdependencies, and the management of project risks. Perform detailed

### Pharmaceutical Information Specialist - Merck & Co., Inc.
- Location: CHN - Shanghai - Shanghai (Tower A) (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-05
- 401(k) match: listed (not source-backed)
- Apply: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/CHN---Shanghai---Shanghai-Tower-A/Pharmaceutical-Information-Specialist_R401276-1
- Excerpt: Pharmaceutical Information Specialist CHN - Shanghai - Shanghai (Tower A) posted: Posted 7 Days Ago

### Vice President, Pharmaceutical Development - Kymera Therapeutics Inc
- Location: Watertown, MA (unspecified)
- Salary: $315K-$395K
- Posted: 2026-05-26
- 401(k) match: listed (not source-backed)
- Apply: https://www.kymeratx.com/careers-culture/working-at-kymera/?gh_jid=7748334003#open-positions
- Excerpt: Vice President, Pharmaceutical Development Watertown, MA Who we are: Kymera is a clinical-stage biotechnology company pioneering the field of targeted protein degradation (TPD) to develop medicines that address critical health problems and have the potential to dramatically improve patients' lives. Kymera is deploying TPD to address disease targets and pathways inaccessible with conventional therapeutics. Having advanced the first degrader into the clinic for immunological diseases, Kymera is focused on building an industry-leading pipeline of oral small molecule degraders to provide a new generation of convenient, highly effective therapies for patients with these conditions. Founded in 2016, Kymera has been recognized as one of Boston's top workplaces for the past several years. For more information about our science, pipeline and people, please visit www.kymeratx.com or follow us on X (formerly Twitter) or LinkedIn . How we work: - PIONEER : We are courageous, resilient and rigorous in our mission to improve patients' lives through our revolutionary degrader medicines. - COLLABORATE : We value trust + transparency from everyone. Our goals are shared, our decisions data-driven and our camaraderie genuine. - BELONG : We recognize our differences, inviting curiosity and inclusivity, so that our people are valued, seen, and heard. How you'll make an impact: - Define and lead the company's pharmaceutical development strategy across the portfolio, ensuring alignment with corporate priorities and development timelines - Provide strategic leadership for preformulation, biopharmaceutics, and formulation development activities supporting discovery, preclinical, and clinical-stage programs - Champion innovation in formulation sciences and enabling technologies to

### Pharmaceutical Operator - Ashland Global
- Location: US-OH-COLUMBUS (ATLAS) (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-27
- Apply: https://ashland.wd12.myworkdayjobs.com/AshlandCareers1/job/US-OH-COLUMBUS-ATLAS/Pharmaceutical-Operator_2026-0250
- Excerpt: Pharmaceutical Operator US-OH-COLUMBUS (ATLAS) posted: Posted 16 Days Ago

### Pharmaceutical Information Manager - Merck & Co., Inc.
- Location: CHN - Shanghai - Shanghai (Trading) (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-04
- 401(k) match: listed (not source-backed)
- Apply: https://msd.wd5.myworkdayjobs.com/SearchJobs/job/CHN---Shanghai---Shanghai-Trading/Pharmaceutical-Information-Manager_R401755-2
- Excerpt: Pharmaceutical Information Manager CHN - Shanghai - Shanghai (Trading) posted: Posted 8 Days Ago

### Senior Medical Director Clinical Development Neuroscience - Arvinas Inc
- Location: Remote, Hybrid, New Haven - CT (hybrid)
- Salary: Not disclosed
- Posted: 2026-04-10
- Hires in: CT
- Apply: https://job-boards.greenhouse.io/arvinas/jobs/7696313003
- Excerpt: Senior Medical Director Clinical Development Neuroscience Remote, Hybrid, New Haven - CT Arvinas is a clinical-stage biotechnology company dedicated to improving the lives of patients suffering from debilitating and life-threatening diseases through the discovery, development, and commercialization of therapies that degrade disease-causing proteins. Arvinas uses its proprietary PROTAC® Discovery Engine platform to engineer proteolysis targeting chimeras, or PROTAC® targeted protein degraders, that are designed to harness the body's own natural protein disposal system to selectively and efficiently degrade and remove disease-causing proteins. Arvinas is currently progressing multiple investigational drugs through clinical development programs, including ARV-102, targeting LRRK2 for neurodegenerative diseases; ARV-806, targeting KRAS G12D for mutated cancers, including pancreatic, colorectal, and non-small cell lung cancers; ARV-393, targeting BCL6 for relapsed/refractory non-Hodgkin Lymphoma; ARV-027, targeting the polyglutamine-expanded androgen receptor, or polyQ-AR, in skeletal muscle; and vepdegestrant, targeting the estrogen receptor for patients with locally advanced or metastatic ER+/HER2- breast cancer. On August 8 th 2025, the U.S. Food and Drug Administration (FDA) accepted the New Drug Application (NDA) for vepdegestrant- an investigational, orally bioavailable PROTAC estrogen receptor degrader- for its use as a monotherapy in the treatment of adults with estrogen receptor-positive (ER+), human epidermal growth factor receptor 2-negative (HER2-), ESR1-mutated advanced or metastatic breast cancer previously treated with endocrine-based therapy. In September 2025, Arvinas and Pfizer announced their plan to jointly select a third party for the out-licensing and commercialization of vepdegestrant. In April 2024, Arvinas entered into a transaction with Novartis, including a global license agreement for the development

### Pharmaceutical Sales Representative- Glendale,CA - GSK plc
- Location: 4 Locations (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-02
- 401(k) match: listed (not source-backed)
- Apply: https://gsk.wd5.myworkdayjobs.com/GSKCareers/job/USA---California---Los-Angeles/Pharmaceutical-Sales-Representative--Glendale-CA_441304
- Excerpt: Pharmaceutical Sales Representative- Glendale,CA 4 Locations posted: Posted 10 Days Ago

### DMPK Scientist - Arvinas Inc
- Location: Remote, Hybrid, New Haven - CT (hybrid)
- Salary: Not disclosed
- Posted: 2026-05-06
- Apply: https://job-boards.greenhouse.io/arvinas/jobs/7725520003
- Excerpt: DMPK Scientist Remote, Hybrid, New Haven - CT Arvinas is a clinical-stage biotechnology company dedicated to improving the lives of patients suffering from debilitating and life-threatening diseases through the discovery, development, and commercialization of therapies that degrade disease-causing proteins. Arvinas uses its proprietary PROTAC Discovery Engine platform to engineer proteolysis targeting chimeras, or PROTAC targeted protein degraders, that are designed to harness the body's own natural protein disposal system to selectively and efficiently degrade and remove disease-causing proteins. Arvinas is currently progressing multiple investigational drugs through clinical development programs, including ARV-102, targeting LRRK2 for neurodegenerative diseases; ARV-806, targeting KRAS G12D for mutated cancers, including pancreatic, colorectal, and non-small cell lung cancers; ARV-393, targeting BCL6 for relapsed/refractory non-Hodgkin Lymphoma; ARV-027, targeting the polyglutamine-expanded androgen receptor, or polyQ-AR, in skeletal muscle; and vepdegestrant, targeting the estrogen receptor for patients with locally advanced or metastatic ER+/HER2- breast cancer. On August 8 th 2025, the U.S. Food and Drug Administration (FDA) accepted the New Drug Application (NDA) for vepdegestrant- an investigational, orally bioavailable PROTAC estrogen receptor degrader- for its use as a monotherapy in the treatment of adults with estrogen receptor-positive (ER+), human epidermal growth factor receptor 2-negative (HER2-), ESR1-mutated advanced or metastatic breast cancer previously treated with endocrine-based therapy. In September 2025, Arvinas and Pfizer announced their plan to jointly select a third party for the out-licensing and commercialization of vepdegestrant. In April 2024, Arvinas entered into a transaction with Novartis, including a global license agreement for the development and commercialization of the

### Associate Director, Clinical Pharmacology - Crinetics Pharmaceuticals INC
- Location: Remote (remote)
- Salary: $166K-$208K
- Posted: 2026-05-12
- 401(k) match: listed (not source-backed)
- Apply: https://crinetics.wd12.myworkdayjobs.com/CrineticsCareers/job/Remote/Associate-Director--Clinical-Pharmacology_JR000603
- Excerpt: Associate Director, Clinical Pharmacology Remote Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. We are driven by science with a patient-centric and team-oriented culture. Crinetics is known for its inclusive workplace culture. We are also a dog-friendly workplace. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully-integrated endocrine company from discovery to patients. Join our team as we transform the lives of others. Position Summary: The Associate Director, Clinical Pharmacology will be responsible for developing clinical pharmacology strategy suitable for target product profile (TPP) and clinical development plan (CDP), leading the design, execution, interpretation, and reporting of Phase 1 clinical pharmacology studies, and serve as clinical pharmacology lead on studies and project teams. The work will support projects at various stages of development thereby allowing the selected candidate to play an active role in our drug discovery and development efforts to advance therapeutics for rare endocrine disorders and endocrine-related cancers. This is a unique opportunity to work with a proven and well-funded drug discovery and development team in a small company environment in the heart of

### Pharmaceutical Laboratory Analyst - Ashland Global
- Location: US-OH-COLUMBUS (ATLAS) (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-20
- Apply: https://ashland.wd12.myworkdayjobs.com/AshlandCareers1/job/US-OH-COLUMBUS-ATLAS/Pharmaceutical-Laboratory-Analyst_2026-0235
- Excerpt: Pharmaceutical Laboratory Analyst US-OH-COLUMBUS (ATLAS) posted: Posted 23 Days Ago

### Senior Director, Clinical Pharmacology - Crinetics Pharmaceuticals INC
- Location: Remote (remote)
- Salary: $238K-$297K
- Posted: 2026-06-08
- 401(k) match: listed (not source-backed)
- Apply: https://crinetics.wd12.myworkdayjobs.com/CrineticsCareers/job/Remote/Senior-Director--Clinical-Pharmacology_JR000637
- Excerpt: Senior Director, Clinical Pharmacology Remote Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. We are driven by science with a patient-centric and team-oriented culture. Crinetics is known for its inclusive workplace culture. We are also a dog-friendly workplace. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully-integrated endocrine company from discovery to patients. Join our team as we transform the lives of others. Position Summary: The Senior Director, Clinical Pharmacology will be a key member of the development team, developing clinical pharmacology strategy suitable for target product profile (TPP) and clinical development plan (CDP), leading the design, execution, interpretation and reporting of Phase 1 clinical pharmacology studies, and serve as clinical pharmacology lead on studies and project teams. The work will support projects at various stages of development thereby allowing the selected candidate to play an active role in our drug discovery and development efforts to advance small molecule therapeutics for rare endocrine disorders and endocrine-related cancers. Essential Job Functions and Responsibilities: These may include but are not limited to: Develop clinical pharmacology strategy and related

### Business Development Associate - Pharmaceutical - Ecolab
- Location: USA - North Carolina - Raleigh (unspecified)
- Salary: Not disclosed
- Posted: 2026-05-12
- Parental leave: 6 weeks (not source-backed)
- Non-birth-parent leave: 6 weeks (not source-backed)
- 401(k) match: listed (not source-backed)
- Apply: https://ecolab.wd1.myworkdayjobs.com/Ecolab_External/job/USA---North-Carolina---Raleigh/Business-Development-Associate---Pharmaceutical_R00293604
- Excerpt: Business Development Associate - Pharmaceutical USA - North Carolina - Raleigh posted: Posted 30+ Days Ago

### Associate Director, Outsourcing & Vendor Governance & Supplier Management (CMC) - Crinetics Pharmaceuticals INC
- Location: San Diego, CA (unspecified)
- Salary: $156K-$204K
- Posted: 2026-05-12
- 401(k) match: listed (not source-backed)
- Apply: https://crinetics.wd12.myworkdayjobs.com/CrineticsCareers/job/San-Diego-CA/Associate-Director--Outsourcing---Vendor-Governance---Supplier-Management--CMC-_JR000544-1
- Excerpt: Associate Director, Outsourcing & Vendor Governance & Supplier Management (CMC) San Diego, CA Crinetics is a pharmaceutical company based in San Diego, California, developing much-needed therapies for people with endocrine diseases and endocrine-related tumors. We were founded by a dedicated team of scientists with the simple belief that better therapies developed from rigorous innovation can lead to better lives. Our work continues to make a real difference in the lives of patients. We have a prolific discovery engine and a robust preclinical and clinical development pipeline. We are driven by science with a patient-centric and team-oriented culture. Crinetics is known for its inclusive workplace culture. We are also a dog-friendly workplace. This is an exciting time to join Crinetics as we shape our organization into the world's premier fully integrated endocrine company from discovery to patients. Join our team as we transform the lives of others. Position Summary: The Associate Director, Outsourcing & Vendor Governance (OVG) & Supplier Management is responsible for the strategic oversight, governance, and performance management of external suppliers supporting the Technical Operations / CMC organization. This role manages a broad and complex network of external partners across development, manufacturing, testing, and supply to ensure reliable, compliant, and cost-effective execution of CMC programs. This position is critical to enabling program success by ensuring external suppliers are effectively selected, governed, and integrated into the company's Technical Operations strategy. The Associate Director serves as a key interface between CMC, Quality, Supply Chain, Finance, and Procurement, and brings deep experience

### Pharmaceutical Sales Representative - Raleigh-Durham NC - IQVIA
- Location: 2 Locations (unspecified)
- Salary: Not disclosed
- Posted: 2026-06-11
- 401(k) match: listed (not source-backed)
- Apply: https://iqvia.wd1.myworkdayjobs.com/IQVIA/job/Raleigh-NC/Pharmaceutical-Sales-Representative---Raleigh-Durham-NC_R1550762
- Excerpt: Pharmaceutical Sales Representative - Raleigh-Durham NC 2 Locations posted: Posted Yesterday

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