Director, Stability Management, Analytical Development and Quality Control Revolution MedicinesDirector, Stability Management, Analytical Development and Quality ControlRedwood City, California$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.
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.
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.
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.
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 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.
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.
Entry-Level Quality Control (QC) Analyst Qnity ElectronicsEntry-Level Quality Control (QC) AnalystHayward, CaliforniaHands-on experience with TGA, UV-Vis, and titration instruments• Strong collaboration skills and ability to work effectively with production teams• Understanding of chemical hygiene and safe laboratory practices• Ability to manage time effectively and maintain good sample turnaround performance• Curious mindset with eagerness to learn QC processes, analytical techniques, and new instruments/technologies• Strong organizational, problem-solving, and continuous improvement mindset. Basic chemistry lab experience (academic or internship acceptable)• Familiarity with analytical techniques such as UV-Vis, titration, or thermal analysis preferred• Proficiency in Microsoft Excel for data processing and analysis• Strong attention to detail and documentation skills• Ability to work both independently and in a team environment.
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.
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.
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 BaxterAnalyst II Quality Control LabHayward, CaliforniaBaxter 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. Use laboratory instrumentation, including KF Titrator, DSC, HPLC, Particle Size Analyzer and Tensile Tester, along with computer systems to collect, record and analyze data.
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.
Seasonal Quality Inspector - Daly City, CA See's Candies, Inc.Seasonal Quality Inspector - Daly City, CADaly City, CASee'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). Job Description Summary: The Quality Inspector is responsible for ensuring the weight, appearance, and overall quality of confectionery products at various stages of the manufacturing, packing, and logistics processes.
Incoming Quality Inspector (2:00Pm - 10:30Pm) Atomic MachinesIncoming Quality Inspector (2:00Pm - 10:30Pm)Emeryville, 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.