Director, Stability Management, Analytical Development and Quality Control Revolution Medicines IncDirector, Stability Management, Analytical Development and Quality ControlRedwood City, CA$211,000–$264,000 / yearThe 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. Collaborate cross-functionally with teams in drug substance, drug product, supply chain, quality, regulatory, sourcing and other related team to ensure alignment of stability design and achieve stability study objectives.
Senior QA Specialist, Global Document Control Management Revolution Medicines, Inc.Senior QA Specialist, Global Document Control ManagementRedwood City, CA$120,000–$150,000 / yearThe 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. Support strategic document management initiatives, including workflow optimization, system enhancements, document migrations, periodic reviews, global expansion activities, training programs, and process improvement projects.
NewQuality Control Analytical Chemist MEDTERIALS INCQuality Control Analytical ChemistSan Carlos, CAFull timeb) Independently perform other analytical assays including Particle Size Analysis, Karl Fischer titration, Differential Scanning Calorimetry, Fluorescence Spectroscopy, following the company’s Test Methods and GMP regulations. Minimum requirements are a Bachelor’s degree (BS) in Chemistry with at least four years GMP pharmaceutical industry experience or a Master’s degree (MS) in Analytical Chemistry or other Chemistry field with at least two years GMP pharmaceutical industry experience.
TEMP Quality Control Manager CytomX TherapeuticsTEMP Quality Control ManagerSouth San Francisco, California$67–$76 / hourAs part of this commitment, we (and the agencies we work with) will assist individuals who have a disability with any reasonable accommodation requests related to employment, including completing the application process, interviewing, completing any pre-employment testing, participating in the employee selection process, and/or to perform essential job functions where the requested accommodation does not impose an undue hardship. Director, Quality Op & Compliance Department : Quality Position Type : Full-time, Non-Exempt, Available from May 15, 2026 through March 15, 2027 About CytomX Therapeutics: CytomX Therapeutics, Inc. is committed to changing the treatment of cancer with our novel PROBODY® therapeutic platform.
Senior QA Specialist, Global Document Control Management Revolution MedicinesSenior QA Specialist, Global Document Control ManagementRedwood City, CaliforniaLeveraging its differentiated RAS(ON) tri-complex inhibitor platform, the company is advancing a broad, integrated portfolio of oral RAS(ON) inhibitors designed to directly target the active, cancer-driving state of RAS. Support strategic document management initiatives, including workflow optimization, system enhancements, document migrations, periodic reviews, global expansion activities, training programs, and process improvement projects.
Senior QA Specialist, Global Document Control Management Revolution Medicines IncSenior QA Specialist, Global Document Control ManagementRedwood City, CA$90,000–$108,000 / yearThe 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. Support strategic document management initiatives, including workflow optimization, system enhancements, document migrations, periodic reviews, global expansion activities, training programs, and process improvement projects.
Senior Scientist, Analytical Development and Quality Control - Early Phase Nurix Therapeutics IncSenior Scientist, Analytical Development and Quality Control - Early PhaseBrisbane, CA$162,000–$186,000 / yearThe Senior Scientist will be responsible for drug product (DP) analytical development, including method development, oversight of method validation at CDMOs, and lifecycle management in support of Nurix's oncology and inflammation & immunology (I&I) programs. The ideal candidate will have expertise in chromatographic and dissolution method development, stability studies, and phase-appropriate validation and control strategies, along with demonstrated experience supporting late-phase development and regulatory submissions.
Senior Scientist, Analytical Development and Quality Control Drug Product Nurix Therapeutics IncSenior Scientist, Analytical Development and Quality Control Drug ProductBrisbane, CA$161,110–$185,618 / yearThe Senior Scientist will be responsible for drug product (DP) analytical development, including method development, oversight of method validation at CDMOs, and lifecycle management in support of Nurix's oncology and inflammation & immunology (I&I) programs. The ideal candidate will have expertise in chromatographic and dissolution method development, stability studies, and phase-appropriate validation and control strategies, along with demonstrated experience supporting late-phase development and regulatory submissions.
Document Control & Quality Systems Administrator Noctrix HealthDocument Control & Quality Systems AdministratorPleasanton, CaliforniaThis role will manage document lifecycle activities, training administration, calibration records, supplier documentation, record retention, finished goods documentation, and other critical quality system activities while identifying opportunities to improve efficiency and compliance. This individual will serve as the primary administrator for controlled documents, employee training records, quality records, and the electronic Quality Management System (eQMS), ensuring information remains accurate, current, traceable, compliant, and inspection-ready.
Senior Manager, Quality Control Vir BiotechnologySenior Manager, Quality ControlSan Francisco, CA$142,500–$199,000 / yearThe Senior Manager, Technical Operations Quality Control, is responsible for executing and operationalizing QC strategy across assigned programs and external testing partners (e.g., CDMOs/CTLs) from Phase 1 through commercialization. The Senior Manager partners cross-functionally with Quality, Technical Operations, Regulatory, and Analytical Development to deliver program milestones, maintain inspection readiness, and support global regulatory submissions.
Senior Manager, Quality Control Vir Biotechnology IncSenior Manager, Quality ControlSan Francisco, CA$142,500–$199,000 / yearThe Senior Manager, Technical Operations Quality Control, is responsible for executing and operationalizing QC strategy across assigned programs and external testing partners (e.g., CDMOs/CTLs) from Phase 1 through commercialization. The Senior Manager partners cross-functionally with Quality, Technical Operations, Regulatory, and Analytical Development to deliver program milestones, maintain inspection readiness, and support global regulatory submissions.
Sr. Director, Analytical Development and Quality Control AllakosSr. Director, Analytical Development and Quality ControlRedwood City, CaliforniaYour Role: Provide technical leadership and guidance across CMC development disciplines to all outsourced analytical methods and testing activities by providing clear objectives for multiple CDMO partners, assess all experimental plans and results, and coordinate future work to achieve desired development and manufacturing expectations. Position Summary: As a member of the Allakos team you will have the opportunity to provide direction and oversight of technical activities associated with methods development, qualification, and validation in support of development of Allakos’ biologics therapeutics targeting eosinophil and mast cell-driven diseases.
Quality Control Medical Writing Serene Healthcare StaffingQuality Control Medical WritingSan Francisco, CaliforniaAdditionally, if applicable, please explicitly state that the candidate is open to immediate relocation since these are IN-OFFICE in SF positions. Nice to Have Skills for Role: Familiarity with structured content formats like XML or JSON.
Senior Manager, Quality Control Vir Biotechnology, Inc.Senior Manager, Quality ControlSan Francisco, CA$142,500–$199,000 / yearThe Senior Manager, Technical Operations Quality Control, is responsible for executing and operationalizing QC strategy across assigned programs and external testing partners (e.g., CDMOs/CTLs) from Phase 1 through commercialization. The Senior Manager partners cross-functionally with Quality, Technical Operations, Regulatory, and Analytical Development to deliver program milestones, maintain inspection readiness, and support global regulatory submissions.
Quality Operations Program Manager - Document Control Veeva Systems IncQuality Operations Program Manager - Document ControlPleasanton, CARemote$100,000–$150,000 / yearServe as System Administrator of Veeva's internal electronic Document Management System (eDMS), responsible for system configuration, user administration, lifecycle management, and continuous improvement of the system and its governed processes. We're not just any public company - we made history in 2021 by becoming a public benefit corporation (PBC), legally bound to balancing the interests of customers, employees, society, and investors.
Senior Scientist, Analytical Development And Quality Control - Drug Product Nurix Therapeutics, Inc.Senior Scientist, Analytical Development And Quality Control - Drug ProductBrisbane, CA$162,000–$186,000 / yearThe Senior Scientist will be responsible for drug product (DP) analytical development, including method development, oversight of method validation at CDMOs, and lifecycle management in support of Nurix's oncology and inflammation & immunology (I&I) programs. The ideal candidate will have expertise in chromatographic and dissolution method development, stability studies, and phase-appropriate validation and control strategies, along with demonstrated experience supporting late-phase development and regulatory submissions.
Senior Scientist, Analytical Development And Quality Control - Early Phase Nurix Therapeutics, Inc.Senior Scientist, Analytical Development And Quality Control - Early PhaseBrisbane, CA$162,000–$186,000 / yearThe Senior Scientist will be responsible for drug product (DP) analytical development, including method development, oversight of method validation at CDMOs, and lifecycle management in support of Nurix's oncology and inflammation & immunology (I&I) programs. The ideal candidate will have expertise in chromatographic and dissolution method development, stability studies, and phase-appropriate validation and control strategies, along with demonstrated experience supporting late-phase development and regulatory submissions.
Quality System Document Control Administrator LancesoftQuality System Document Control AdministratorSanta Clara, CA$35As a QMS & Document Control Specialist, you will support the effectiveness of the site Quality Management System (QMS) by ensuring controlled documents, change management processes, and training activities are executed accurately and in compliance with regulatory requirements. This role is a key contributor to maintaining an audit-ready state, improving process efficiency, and enabling cross-functional teams to implement changes effectively in a regulated environment.
Quality Inspector Sterling Engineering, Inc.Quality InspectorMilpitas, CA$24–$25 / hourThis role is responsible for inspecting products, accurately documenting inspection results, and performing a high volume of data entry to support quality records and manufacturing compliance. The ideal candidate has prior experience working in a clean room, is comfortable wearing full clean room PPE for the duration of their shift, and has strong computer and data entry skills.
Seasonal Quality Inspector - Daly City, CA See’s CandiesSeasonal Quality Inspector - Daly City, CADaly City, CaliforniaSee's is an EOESee’s will consider for employment qualified applicants with criminal histories in a manner consistent with the requirements of applicable local, state or federal law (including San Francisco Ordinance #131192 and Los Angeles Municipal Code 189.00). The roles are scheduled tocommencein September/October and conclude in December, with an orientation date set for September .Seasonal employees are expected toworka full-time schedule of 40 hours per week.