Senior R&D QA Lead — GMP Batch & Clinical Supply
Allergan
AbbVie is seeking a Senior R&D Quality Officer within the Product Development Quality Assurance (PDQA) team. This role ensures timely review and disposition of batch documentation for NBE, NCE, and ATMP programs across TPMs and AbbVie sites, upholding GMP standards and regulatory requirements. The position provides strategic QA leadership, mentors junior staff, and drives continuous improvement in clinical supply quality across global operations. #J-18808-Ljbffr Allergan
- ...seeking an Associate Director, GMP Quality to oversee GMP activities for clinical and commercial products, including review of batch records and supplier... ...with CMC, Regulatory, and Supply Chain functions and may involve... ...in FDA-regulated GMP QA, NDA/BLA submissions, and...Suggested
$275k - $300k
...potential first‑in‑class clinical asset and complemented... ...autoimmune disease.Our lead asset is being... ...‑term potential of our R&D pipeline. At Lakefront,... ...OPPORTUNITYWe are seeking a Senior Counsel, Clinical/R&D Legal... ...business development, supply, services, consulting,...SeniorContract workWork at officeRemote work- ...and disposition of batch documentation to... ...uninterrupted clinical supply, advance the R&D pipeline, and maintain... ...and global GMP requirements. The... ...Description The Senior R&D Quality Officer... ...role applies deep QA expertise and GMP... ...GMP compliance. Lead deviation and investigation...Senior
- ...Lakefront Biotherapeutics seeks a Senior Counsel, Clinical/R&D Legal to own core legal support for clinical operations, manufacturing, and regulatory affairs. The role offers autonomy and partnership with senior stakeholders, with growth into strategic licensing, AI-driven...Senior
- ...Nurix Therapeutics is a clinical stage biopharmaceutical company focused on the discovery... .... About the Position: The Senior Manager, Supply Chain Quality Assurance is responsible... ...providers to ensure compliance with applicable GMP, GDP, GCP (where applicable) and...SeniorFull timeContract work
- ...ensuring high-quality clinical supplies that are compliant... ...to patients. The Senior Manager, Clinical Product... ...across AbbVie R&D functions and... ...oversight for the RDQA QA organization; includes... ...timelines Lead complex global cross... ...global requirements for GMP (D, EU, US) is...SeniorFull timeTemporary workLocal areaWorldwide
$142.5k - $199k
...Biotechnology, Inc. is a clinical-stage... ...OPPORTUNITYThe Senior Manager, Technical... ...organization strategy. Lead QC activities... ...QC performance, supply continuity, and... ...data, batch records, and supporting... ...execution of QC GMP processes (deviations... ...with QA. Coordinate QC documentation...SeniorFull timeContract workWork at officeWork visa3 days per week$160k - $180k
Olema Oncology is a clinical-stage... ...line data from our lead program expected later... ...Associate Director GMP QualityAs the Associate... ...Certificate of Analysis, Batch Disposition, Person... ...CMC, Regulatory and Supply Chain to prepare... ...Pharmaceutical GMP / GMP QA role Experience...Work experience placementWork at officeFlexible hours$240k - $300k
...drugs. We are advancing a clinical‐stage pipeline of... ...Summary:We are seeking a Senior Director of GMP Quality Assurance (QA) to serve as a senior quality... ...responsible for developing, leading, and executing the global... ...manufacturing, testing, and supply activities, including...SeniorContract work- ...San Francisco seeks an experienced Clinical Project Manager to independently lead global clinical trial programs from... ...to closeout. You will partner with R&D, Regulatory, Quality, and Marketing... ...and study execution while ensuring GMP/GCP compliance and patient safety....Senior
- Catalent is seeking an Account Director for Clinical Supply Services. This remote, field-based role focuses on driving annual sales, expanding the customer base, and managing high-level relationships across global accounts. You will participate in strategic account meetings...SeniorRemote jobContract work
$240k - $300k
...drugs. We are advancing a clinical‑stage pipeline of... ...Summary We are seeking a Senior Director of GMP Quality Assurance (QA) to serve as a senior quality... ...responsible for developing, leading, and executing the global... ...manufacturing, testing, and supply activities, including...SeniorContract work$109k - $135k
...peptide drugs. We are advancing a clinical‐stage pipeline of... ...motivated entry level Clinical Supplies Professional with experience in... ...operations at clinical supply vendors, batch record review, distribution... ...regulationsWorks closely with QA to ensure compliance with IP documentation...SeniorContract workWork at officeRemote workFlexible hoursShift work$170k - $212k
...Medicines is a late-stage clinical oncology company... .... The company’s R&D pipeline comprises... ...role as a technical lead within the Drug... ...management of redundant supply and geographic... ...protocols, manufacturing batch records, and... ...current ICH guidelines, GMP, and relevant...SeniorWork experience placement$190k - $240k
...for the Director of Clinical Quality Assurance... ...Development, Clinical Supply Chain, Medical... ...Alumis. The Clinical QA Director is... ...experience in successfully leading assigned activities... ...along the way. Seniority level ~ Seniority... ...Associate Director, GMP Quality Assurance...Full time$140k - $190k
...and APRIL may prove clinically meaningful. Vera Therapeutics... ...every day. We lead with empathy, act... ...Position Summary:The Senior Manager, Quality Assurance (QA), will report to the... ...DS.Review executed batch records and associated... ....Review and approve GMP documentation such...SeniorContract workFor contractorsWork experience placementFlexible hours$164k - $205k
Revolution Medicines is a late-stage clinical oncology company developing... ...cancers. The company’s R&D pipeline comprises RAS(ON) inhibitors... ...are seeking an experienced Senior Manager, Commercial Supply Chain, Serialization & Traceability to lead global serialization and...SeniorFull timeLocal area$160k - $180k
Olema Oncology seeks a Senior Manager, GCP Clinical Quality in San Francisco, CA to ensure compliance in clinical development. This hybrid role requires 2 days a week on-site work and up to 25% travel. The ideal candidate will have a Bachelor’s degree in a scientific discipline...2 days per week- BioMarin is a leading rare disease biotechnology company... ...our drugs for use in clinical trials and for scaling... ...San Rafael, CA (HQ) The Senior Director, Integrated Planning... ...across demand, supply, inventory, capacity, and... ...demand variability, small batches, long lead times, and...SeniorImmediate startWorldwide2 days per week
$230k - $300k
...by a potential first‑in‑class clinical asset and complemented by an exciting... ...in autoimmune disease.Our lead asset is being developed for... ...long‑term potential of our R&D pipeline. At Lakefront, we focus... ...RoleWe are seeking a Director or Senior Director of Clinical...SeniorContract work- Genentech, based in South San Francisco, is seeking a strategic Clinical Operations leader to drive early development programs... ...-performing teams in a matrix environment, influencing senior stakeholders across R&D and operations. The role requires deep regulatory...Senior
- Structure Therapeutics in South San Francisco is seeking a Senior Director of GMP Quality Assurance to lead the global GMP QA strategy, ensuring compliance and overseeing quality operations. The successful candidate will have over 15 years of experience in quality management...
- ...oriented GxP and Regulatory QA Lead to join our fast-... ...compliance of company's clinical/non-clinical operations... ...assignments, GxP (GLP/GCP/GMP) compliance and FDA 21... ...-functional teams (R&D, Clinical, Non-clinical... ...Engineering or related fields. Seniority Level Mid-Senior level...Full timeWork at office
$230k - $300k
...programs, led by a potential first‑in‑class clinical asset and complemented by an exciting... ...preclinical portfolio in autoimmune disease.Our lead asset is being developed for severe immune... ...expand the long‑term potential of our R&D pipeline. At Lakefront, we focus on advancing...Senior- Rigel Pharmaceuticals Inc is seeking a Senior Manager Quality Assurance Quality Operations to oversee GMP QA activities for commercial and clinical products manufactured and tested... ...will ensure manufacturing readiness, batch disposition, change management and QC...Senior
- iRhythm Technologies, Inc. is seeking a Manager of Clinical Quality to oversee and enhance the quality of clinical operations. This role involves managing a team of 20-25 quality assurance clinical technicians, ensuring performance meets operational standards, and maintaining...Senior
- Dolby is seeking a QA Manager for the Dolby Cinema QA group in San Francisco. You will lead test strategy, lab readiness, and end-to-end testing across complex imaging programs involving projectors, cinema servers, and networking. This hands-on leadership role requires...Senior
- Hinge Health is seeking a QA Associate Manager to join the Growth Marketing Operations team in San Francisco. You will lead testing and validation across email, SMS, push, and in-app messaging, ensuring segmentation accuracy and data integrity before deployment. You will...Senior
- A leading biotech company is seeking a self-motivated GxP and Regulatory QA Lead to oversee compliance within clinical and non-clinical operations. The role requires at least 7 years of relevant experience in Quality Assurance within the pharmaceutical or biotechnology...SeniorFull time
- POSITION SUMMARY The Senior Manager Quality... ...day to day GMP Quality Assurance... ...commercial and clinical products manufactured... ...testing support batch disposition... ...Technical Operations Supply Chain Regulatory... ...Management Lead Quality review and... ...comprehensive QA review of executed...SeniorContract workFlexible hours
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