Manager I, Quality Control Baxter International IncManager I, Quality ControlHayward, CA$112,000–$154,000 / yearWork closely with manufacturing and product development teams and participate in pro-active functions that impact production, increase efficiency, solve problems, generate cost savings, improve quality and provide new product support. Strong understanding of chemistry, environmental monitoring, microbiological (e.g., pyrogen, bioburden), sterilization and/or real-time stability testingMust know quality laboratory operations and government regulations pertaining to pharmaceutical and medical device manufacturing labs.
Scientist, Reagent Manufacturing & Quality Control AccuScan SciencesScientist, Reagent Manufacturing & Quality ControlMilpitas, CaliforniaDescription The Scientist, Reagent Manufacturing & Quality Control (QC), is responsible for the production, characterization, and release testing of enzymes and critical reagents to support internal R&D activities and external diagnostic kit manufacturing, including in vitro diagnostic (IVD) products. The position is highly hands-on and requires execution of controlled manufacturing processes, analytical testing, and rigorous documentation practices to support design control, traceability, and regulatory compliance.
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.
Quality Control Technician- Swing shift Sakuu CorpQuality Control Technician- Swing shiftSan Jose, CAPerform a variety of tasks including setting up test equipment, performing QC tests using variety of metrology equipment, visual and microscopic inspection, data compiling and reporting, equipment calibration and maintenance, part cleanings. The responsibilities of a Quality Control Technician are to assist the quality team in guaranteeing the quality of products and services, and to assist in the process of preparing all product certificates of analysis.
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.
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.
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, California$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.
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.
Entry-Level Quality Control (QC) Analyst Qnity ElectronicsEntry-Level Quality Control (QC) AnalystHayward, CaliforniaThis entry-level role involves operating analytical instruments, maintaining chemical safety, collaborating with production teams, and ensuring timely and accurate data reporting. The QC Analyst is responsible for performing routine laboratory testing and supporting quality control activities to ensure products meet established specifications.
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.
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.
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.
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 Nurix Therapeutics, Inc.Senior Scientist, Analytical Development And Quality ControlBrisbane, 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.
Analyst II Quality Control Lab Baxter International IncAnalyst II Quality Control LabHayward, CA$96,000–$132,000 / yearDemonstrates integrity, sound judgment, strong work ethic, intellectual honesty, dedication to quality, eagerness to learn, and drive for continuous improvement and solutionsMust have the following personal attributes: integrity and trust, work ethic, sound judgment, intellectual honesty, pragmatism, courage and conviction. Recruitment Fraud NoticeBaxter has discovered incidents of employment scams, where fraudulent parties pose as Baxter employees, recruiters, or other agents, and engage with online job seekers in an attempt to steal personal and/or financial information.
Incoming Quality Inspector 2:00pm - 10:30pm Atomic Machines IncIncoming Quality Inspector 2:00pm - 10:30pmEmeryville, CA$39–$45 / hourFurthermore, this digital platform is fully programmable in the way 3D printing is digital-but whereas 3D printing produces parts of a single material using a single process, the Matter Compiler technology platform is a multi-process, multi-material system: bits and raw materials go in, and complete, functional micromachines come out. This platform enables new classes of micromachines to be designed and built by providing manufacturing processes and a materials library that are inaccessible to semiconductor manufacturing methods.
CMM Quality Inspectors LaborupCMM Quality InspectorsSan Jose, CA$70,000–$80,000You'll run existing CMM programs and inspect by hand for first article, in-process, and final inspection on complex, tight-tolerance parts bound for aerospace, defense, semiconductor, and medical customers. Inspection runs on Brown & Sharpe (PC-DMIS) and Aberlink Axiom CMMs, backed by micrometers, calipers, and other hand tools.
QUALITY INSPECTOR HORSPOOL & ROMINE MFG CO INCQUALITY INSPECTOROAKLAND, CAFull timeFounded in 1985, HORSPOOL & ROMINE MFG CO INC has built a reputation for delivering high-quality manufacturing solutions that exceed customer expectations. Identify defects and non-conformities, and collaborate with production teams to implement corrective actions.