Director, Quality Control Corcept TherapeuticsDirector, Quality ControlRedwood City, CA$215,300–$253,200 / yearThe pay range that the Company reasonably expects to pay for this headquarters-based position is $215,300-$253,200; the pay ultimately offered may vary based on legitimate considerations, including geographic location, job-related knowledge, skills, experience, and education. With advanced clinical trials in patients with hypercortisolism, solid tumors, ALS and liver disease, Corcept is unlocking the power of cortisol modulation to help address some of the most devastating diseases patients face today.
NewQuality Control Technician ActalentQuality Control TechnicianSan Jose, CA$25–$34 / hourResponsibilities Perform chemical, physical, and instrumental testing on raw materials, in-process, finished, and customer product samples, including volumetric and gravimetric analyses, pH measurements, FTIR, specific gravity (SPG), refractive index (RI), and other instrumental techniques. The technician works with a variety of analytical instruments and techniques, including FTIR, pH meters, volumetric and gravimetric equipment, and tools for specific gravity (SPG), refractive index (RI), IACS, and thermal conductivity measurements.
Quality Control Laboratory Analyst Rose InternationalQuality Control Laboratory AnalystSan Jose, California$26–$32 / hourTemporaryJob Description Required Education • Bachelor's degree in chemistry, Biochemistry, Biology, Pharmaceutical Sciences, or a related field Required Experience / Skills: • Minimum 2 years of relevant laboratory experience in analytical testing, chemistry, biochemistry, pharmaceutical, or related environments • Experience performing routine and non-routine chemical/biochemical analysis of raw materials, in-process materials, and finished products • Knowledge of laboratory procedures, analytical techniques, equipment calibration, and maintenance • Ability to review test data against specifications and identify/report abnormalities • Experience with laboratory documentation, investigations, reports, and SOPs • Strong attention to detail, organization, and problem-solving skills Job Duties: • Conduct routine and non-routine chemical and biochemical analyses according to established procedures • Perform testing related to stability programs, formulation studies, and special laboratory projects • Calibrate, operate, and maintain laboratory and analytical equipment • Document and review test results for compliance with specifications and report abnormalities • Assist with investigations, summaries, reports, and SOP updates • Support analytical and instrument troubleshooting and problem-solving activities • Assist with developing or improving testing methods in accordance with established guidelines. **Please note that all Position start dates and duration are estimates and may be reduced or lengthened based upon a client's business needs and requirements.**.
Director, Stability Management, Analytical Development and Quality Control Revolution MedicinesDirector, Stability Management, Analytical Development and Quality ControlRedwood City, CaliforniaThe 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, Inc.Director, 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, CaliforniaThe 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.
Document Control & Quality Systems Administrator Noctrix HealthDocument Control & Quality Systems AdministratorPleasanton, California$120,000–$140,000 / yearThis 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.
Incoming Quality Control Technician Capstan MedicalIncoming Quality Control TechnicianSanta Cruz, CaliforniaThis role supports incoming quality control activities, performs visual and dimensional inspections, reviews quality documentation, assists with nonconformance investigations, and helps maintain accurate quality records in a Class III medical device manufacturing environment. Based in Santa Cruz, our unique workspace blends cutting-edge Bay Area innovation with a lifestyle-driven environment near trails, beaches, and open space—creating the perfect place to do meaningful, career-defining work.
Office Administrative and Customer Support - Quality System Document Control Administrator MindlanceOffice Administrative and Customer Support - Quality System Document Control AdministratorSanta Clara, CA$33–$35 / hourAs 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.
Senior QA Specialist, Global Document Control Management Revolution MedicinesSenior QA Specialist, Global Document Control ManagementRedwood City, CaliforniaThe 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.
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.
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 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.
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.
Seasonal Quality Inspector - South San Francisco, CA See's Candies, Inc.Seasonal Quality Inspector - South San Francisco, CASouth San Francisco, 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.
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.
Quality Inspector No More NeedlesQuality InspectorFremont, CaliforniaGENERAL INFORMATION Position Title: Quality Inspector (II, III, or Senior) Department: Quality Assurance Reports to: Quality Engineering Purpose of the Job This Quality Inspector position will report to Quality Engineering. Main responsibilities include performing incoming inspections of materials/parts/products and reviewing and approval of manufacturing batch records and inspection records.
Quality Inspector Apidel TechnologiesQuality InspectorSanta Clara, CAContractorThis role inspects inventory for acceptable visual condition and dimensional specifications and is responsible for the restoration and preservation of specific materials, as well as the assembly of components and modification of finished goods. Work with external customers, internal customers, suppliers, and business leadership as needed to meet goals and communicate performance.