89 Quality Assurance And Compliance jobs in San Francisco.

Redwood City

• Skills: Clinical Quality, GCP, audit plans, regulatory standards, clinical trials, biotechnology, risk assessment, communication skills, compliance guidance, training development
• Experience: 8+ years’ experience working within GCP in a pharmaceutical or biologics environment.
• Type: Full-time

San Francisco

• Skills: Validation, Commissioning, Qualification, Document Development, Regulated Industry, Technical Problem-Solving, Project Management, Microsoft Word, Microsoft Excel, ISPE Baseline Guide 5
• Experience: 4-16 years’ experience performing commissioning and/or qualification activities in a regulated industry
• Type: Full-time

Burlingame

• Skills: Functional Safety, Quality Management Systems, ISO 26262, Traceability analysis, Safety mechanisms, Internal/external audits, DIA, Safety Manuals, FMEA reports, 3rd party auditors
• Experience: 10+ years of experience in CPU, DSP or GPU development; 5+ years of experience in functional safety development.
• Type: Full-time

Pleasanton

• Skills: quality assurance, SaaS, Vault CRM, functional testing, production deployment, life sciences, customer success, public benefit corporation, mission-driven, hands-on position
• Type: Full-time

Foster City

• Skills: Supplier Industrialization, Quality Assurance, Supplier Quality Engineers, Quality System, Continuous Improvements, Regulatory Compliance, Product Quality, Service Quality, Performance Evaluation, Leadership
• Type: Full-time

Alameda

• Skills: Regulatory Affairs, medical devices, 510(k) submissions, CE-Mark, Quality System regulations, ISO 13485, Design Control, Regulatory Intelligence, interpersonal communication skills, organizational skills
• Experience: 2+ years of experience
• Type: Full-time

Mountain View

• Skills: Supplier Quality, PPAP process, APQP, ISO 9001, IATF 16949, Lidar, Radar, camera-based components, Supplier audits, FMEA
• Experience: 7+ years of experience in supplier quality
• Type: Full-time

San Francisco

• Skills: Operations Program Manager, Quality Control, Machine Learning, Generative AI, Quality Control Specialists, Project Management, Analytical Skills, Problem Solving, Team Development, Process Improvement
• Type: Full-time

Fairfield

• Skills: quality assurance, safety, food safety, training, environmental management, customer relations, defective materials, claims, sustainable, packaging
• Experience: 4 years minimum
• Type: Full-time

Alameda

• Skills: GMP Operations, Quality Assurance, Clinical Trials, Contract Manufacturing Organizations, Vendor Management, Regulatory Requirements, Documentation Review, Pharmaceutical Industry, Investigations Coordination, Quality Compliance
• Experience: 7 years related experience with BS/BA, 5 years with MS/MA, or 0 years with PhD.
• Type: Full-time

Palo Alto

• Skills: hardware product quality, consumer electronics, manufacturing processes, supplier relationships, customer satisfaction, cross-functional collaboration, continuous improvement, quality strategy, risk management, global operations
• Experience: 14+ years of professional experience in a senior leadership role
• Type: Full-time

Fremont

• Skills: Quality Management System, 8D, process improvement, SPC, FMEA, Lean manufacturing, internal audits, training, customer quality concerns, manufacturing process
• Experience: Minimum of 5 years of experience in quality engineering or related area in a manufacturing environment
• Type: Full-time

Novato

• Skills: QA oversight, cGMP compliance, batch records, quality assurance, documentation, root cause analysis, manufacturing support, investigation, change control, analytical skills
• Experience: Prior batch record execution or review experience; working knowledge of cGMPs.
• Type: Temporary

Hayward

• Skills: Quality, Technician, Microbiology, Laboratory, Inspection, Quality Assurance, Quality Control, Medical Devices, Healthcare, Regulatory
• Type: Full-time

San Francisco

• Skills: business control, compliance, regulatory requirements, risk management, financial services, consumer protection, internal controls, regulatory landscape, QA program, stakeholders
• Experience: 5+ years in regulatory compliance, risk management, or internal controls within the financial services or fintech sector.
• Type: Full-time

Menlo Park

• Skills: Quality Assurance, Automation, Testing, Engineering, Product Development, Team Management, Metrics, Best Practices, Software Quality, Testability
• Experience: 8+ years of relevant QA/testing automation experience, 3+ years of management experience
• Type: Full Time

Alameda

• Skills: Quality Engineering, Medical Devices, Testing Methodology, Inspection Documentation, Continuous Improvement, Supplier Activities, Engineering Change Orders, QC Process, Quality Management System, Regulations
• Experience: 3+ years of quality engineering or relevant experience

Sunnyvale

• Skills: Quality Engineering, Robotic Surgery, Medical Devices, Manufacturing, Compliance, Team Leadership, Process Improvement, Quality Assurance, Risk Management, Continuous Improvement
• Experience: Minimum 16 years in medical Design, Quality, Manufacturing and/or Engineering. Minimum 8+ years management experience.
• Type: Full-time

Novato

• Skills: Quality Assurance, Computer Systems Validation, Compliance, GxP, Regulatory Standards, Data Integrity, Change Control Management, Analytical Instruments, Software Development Life Cycle, Life-science
• Experience: 8 to 10 years in CSV in the Life-science/regulated industry; 3 to 5 years in Analytical Instruments validation.
• Type: Hybrid

Novato

• Skills: Quality Assurance, Validation, Computer Systems, GxP, Software Development Life Cycle, Change Control Management, Data Integrity, Automation, Risk Assessment, CAPA
• Experience: 8 to 10 years in CSV in the Life-science/regulated industry, 3 to 5 years in Analytical Instruments validation
• Type: Hybrid (minimum 2 days onsite)

Alameda

• Skills: Quality Assurance, ISO, Engineering, Manufacturing, Design Control, Statistical Analysis, Compliance, Medical Devices, Regulated Industry, Project Management
• Experience: 5+ years of relevant experience

San Francisco

• Skills: trade audit, risk management, investment actions, model providers, account management, tax harvesting, portfolio management, trade order systems, communication skills, procedural adherence
• Experience: 3-5 years’ experience with SMA/UMA/portfolio management

South San Francisco

• Skills: Quality Assurance, GCP, GVP, Clinical Trials, Regulatory Compliance, Audit, Risk Assessment, Pharmaceutical Industry, Stakeholder Management, KPI
• Experience: Minimum 12 years of GCP/GVP Quality Assurance experience.
• Type: Full-time

Santa Clara

• Skills: Quality Management System, ISO 9001, Internal audits, Document control, Corrective actions, Process improvement, Quality metrics, FMEA, External audits, Automation
• Experience: Experience building and maintaining a QMS for a semiconductor company.

South San Francisco

• Skills: GMP, validation, quality oversight, biologics, cell therapy, compliance, risk management, technical documentation, regulatory requirements, CAPA
• Experience: 10+ years of experience in a GMP environment; 5+ years in quality or validation roles; 5+ years managing individual contributors.
• Type: Full Time

Sunnyvale

• Skills: Quality Assurance, Medical Device, FDA Regulations, ISO 13485, IEC 62304, Verification and Validation, Software Development Life Cycle, Risk Management, Compliance, Software Testing
• Experience: At least 3-5 years of experience in software quality engineering
• Type: Full-time

South San Francisco

• Skills: quality assurance, Good Clinical Practice (GCP), Good Pharmacovigilance Practice (GVP), compliance, clinical trials, QA professionals, strategic leadership, continuous improvement, patient safety, clinical research

Novato

• Skills: air quality modeling, regulatory guidelines, model input data, model output data, review and QA, state and federal guidance, modeling protocols, scripts development, sustainability, team collaboration
• Experience: 5+ years of air quality modeling experience
• Type: Full-time

Menlo Park

• Skills: Manufacturing Quality Engineer, Quality Management, Vendor Management, Project Performance, Data Center, Leadership, Vendor Audits, Process Management, Training, Operational Readiness
• Experience: 7+ years
• Type: Full Time

San Leandro

• Skills: Quality Control, SOPs, Audits, Inventory Health, Risk Management, Training Programs, Logistics, Operational Quality, Risk Audits, Compliance
• Experience: 1-3 years of experience in quality, logistics, operations, or a related role
• Type: Full-time

Mountain View

• Skills: Quality Assurance, Inspection, Testing, Aerospace, Manufacturing, ISO, Data Analysis, Process Improvement, Documentation, Collaboration
• Type: Full-time

Fremont

• Skills: Quality Manager, quality standards, quality control procedures, inspections, data analysis, improvements, production processes, safety regulations, legal regulations, customer satisfaction

San Leandro

• Skills: Quality Control, Compliance, Inventory Management, Logistics, Audits, Risk Assessment, SOPs, Data Analysis, Continuous Improvement, Facilitation
• Type: Full-time

Santa Clara

• Skills: Quality Management System, reliability strategy, engineering validation, high-volume manufacturing, quality systems, reliability goals, FMEAs, HALT/HASS, root cause investigations, Supplier Quality Assurance
• Experience: 15–20+ years in quality and reliability engineering roles, including leadership positions
• Type: Full-time

San Francisco

• Skills: Quality Assurance, Trust & Risk, customer service, metrics, policy adherence, compliance, process improvement, customer satisfaction, analytical skills, training
• Experience: 5+ years in Operations or contact center environments; at least 3+ years in quality assurance
• Type: Full-time

Milpitas

• Skills: Compliance, Testing, Test Plan, Test Setup, Monitoring, Quality Procedures, Design, Accreditations, Laboratory Equipment, Standards

San Francisco

• Skills: Quality Assurance, Auditing, Clinical Trials, Regulatory Compliance, GCP, SOPs, Risk Management, Clinical Operations, Vendor Management, Inspection Readiness
• Experience: 5-8 years GCP Quality Assurance auditing experience

Sunnyvale

• Skills: quality inspection, dimensional testing, measurement tools, engineering drawings, ISO standards, quality management, non-conformities, supplier performance, quality assurance, process enhancements
• Experience: Minimum 5 years of direct QA/QC experience in manufacturing industries.

Redwood City

• Skills: Quality Management, FDA regulations, ISO 13485, Process Controls, Risk Management, Validation, Continual Improvement, Internal Audits, Statistical Process Control, Change Control

Fremont

• Skills: quality gaps, ISO 13485, batch records, work instructions, SOPs, testing, calibration, non-conforming material, investigations, raw materials
• Experience: 5+ years in reagents or consumables quality

Fremont

• Skills: supervise, inspection, safety, training, compliance, inventory, reporting, monitoring, corrective action, inspection
• Experience: 1-3 years of experience
• Type: Full-time

Fremont

• Skills: supervisor, GMP, safety, inspection, training, coordinator, compliance, inventory, reports, corrective action
• Experience: 1-3 years

Oakland

• Skills: GxP, GCP, GLP, Quality Assurance, Regulatory Compliance, Audit, CAPA, RCA, Quality Management System, Clinical Research
• Experience: At least 10 years within pharmaceutical and/or biotech industry
• Type: Full-time

Hayward

• Skills: Safety, Quality, Compliance, Pharmacovigilance, PV, Regulatory, Audits, Inspection, Deviations, CROs

Fremont

• Skills: quality assurance, QA/QC, GMP, HACCP, QMS, root cause analysis, product quality, compliance, regulatory, team leadership
• Experience: Minimum 5 years of QA/QC experience in a regulated production organization

South San Francisco

• Skills: Clinical Quality Assurance, GCP, Regulatory Compliance, Audits, Risk Management, Quality Systems, FDA Regulations, Monitoring, Documentation, Inspection Readiness
• Experience: Minimum 10 years of Clinical Quality Assurance experience
• Type: Full-time

Novato

• Skills: technology transfer, validation, GMP, project management, regulatory inspections, process improvement, documentation, risk management, cross-functional teams, quality assurance
• Type: full_time

Fremont

• Skills: Quality Management System, CAPA, Non-conformance, Complaints, ISO 13485:2016, 21 CFR 820, Regulatory Compliance, Biotechnology, Medical Device, Quality Systems
• Type: full_time

Menlo Park

• Skills: manufacturing processes, quality control, statistical process control, design for manufacturability, design for testability, failure analysis, product lifecycle management, ISO 9001, supplier quality management, continuous improvement
• Type: full_time

Santa Clara

• Skills: Quality Management System, GxP evaluation, validation, change control, CAPA, ISO 13485, risk management, regulatory compliance, software quality, project management
• Type: full_time

Alameda

• Skills: Supplier Quality Engineering, Quality systems, Regulated medical device, Supplier management, Corrective actions, Risk mitigation, Statistical methods, Quality tools, QSR, ISO 13485
• Type: full_time

Hayward

• Skills: Quality Assurance, ISO/IEC:17025, ISO/IEC:9001, TNI Standards, DOD QSM, audits, regulatory compliance, EHS labs, corrective actions, SOPs
• Type: full_time

Redwood City

• Skills: regulatory compliance, industry standards, ANSI, ISO, UL508A, global expansion, robotics, hardware-agnostic, warehouse automation, compliant solutions

Santa Clara

• Skills: quality assurance, nuclear, audit, ASME NQA-1, ISO 9001, document control, nonconformance management, supplier audits, regulatory compliance, continuous improvement
• Type: full_time

Alameda

• Skills: QHSE, quality management system, safety assurance, integrated management system, OSHA compliance, incident investigation, risk management, continuous improvement, cross-functional collaboration, high-performing teams
• Type: full_time

Santa Clara

• Skills: Quality Operations, Supplier Quality, ISO 13485, FDA Current Good Manufacturing Practices, risk management, manufacturing processes, supplier audits, document control, design changes, KPI metrics
• Type: full_time

Sunnyvale

• Skills: Quality Engineering, electromechanical systems, risk management, design control, design verification, ISO 13485, FDA Quality System Regulations, usability, human factors standards, Design for Reliability
• Type: full_time

San Francisco

• Skills: Document Control, Veeva QualityDocs, Training Program, GxP regulations, Quality Assurance, Document Change Controls, Learning Management System, Compliance, Process Improvement, Documentation
• Type: full_time

Concord

• Skills: medical record auditing, compliance, process improvement, stakeholder engagement, trend analysis, documentation management, regulatory audit, quality improvement, care planning, interdisciplinary team
• Type: full_time

San Ramon

• Skills: quality assurance, regulatory compliance, data reporting, internal audits, performance improvement, controlled documents, corrective action, training compliance, accreditations, medical terminology
• Type: full_time

Oakland

• Skills: environmental compliance, health and safety regulations, EPA, OSHA, audits, permit applications, training, accident investigations, safety consultation, ISO 45001
• Type: full_time

Menlo Park

• Skills: Manufacturing Quality Engineer, Quality Program, Vendor Management, Performance Metrics, Project Performance, Operational Readiness, Field Service Representatives, Corrective Actions, Root Cause Analysis, Team Leadership
• Type: full_time

Petaluma

• Skills: Quality Control, Inspection, Manufacturing, ISO 9001, Statistical Process Control, Lean manufacturing, DMAIC, FMEA, Gage R&R, Mechanical inspection
• Type: full_time

Petaluma

• Skills: Quality Assurance, cGMP, regulatory compliance, batch review, procedures, continuous improvement, investigations, technical support, deviations, quality systems
• Type: contract

Petaluma

• Skills: Quality Assurance, cGMP, document control, batch record review, ISO 9001, ISO 13485, 21 CFR 820, analytical records, QC, compliance
• Type: full_time

Alameda

• Skills: Training Programs, GMP, Quality System, Medical Devices, SOPs, Microsoft Excel, Regulations, Clean Room Standards, Interpersonal Communication, Documentation
• Type: other

Hercules

• Skills: Supplier Quality, Compliance, Risk Assessment Program, Continuous Improvement, Defect Trends, FDA Standards, ISO 13485, Supply Chain Management, Audits, Team Management
• Type: full_time

Sunnyvale

• Skills: Enterprise Data, Analytics, Quality Assurance, Onsite, Information Technology, Software Testing, Regulatory Affairs, Medical Devices, Robotic Surgery, COVID-19 Compliance
• Type: full_time

San Mateo

• Skills: quality management systems, ISO 13485, 21 CFR Part 820, regulatory compliance, supplier quality management, risk management, statistical tools, quality audits, CAPA, quality culture
• Type: full_time

Santa Clara

• Skills: Quality Systems Specialist, CAPA, FDA regulations, ISO13485, Medical Device, Internal Audits, Quality Management System, Data Analysis, Regulatory Compliance, Continuous Improvement
• Type: full_time

Alameda

• Skills: quality engineering, supplier management, inspection techniques, decision making, problem solving, compliance, performance reviews, ASQ certifications, SPC, risk analysis
• Type: full_time

Union City

• Skills: quality management systems, ISO 13485, molecular diagnostics, configuration management, regulatory compliance, clinical validation, cross-functional teams, project management, stakeholder engagement, medical devices
• Type: other

Burlingame

• Skills: Water Quality, Quality Manager, ISO 17025, Laboratory Accreditation, Quality Systems, Health and Safety, Environmental Laboratory, Quality Assurance, Training Programs, Regulatory Standards
• Type: full_time

Sunnyvale

• Skills: Product Compliance, Quality Management System, medical device industry, regulatory requirements, field actions, risk management, surgical medical devices, Cross-functional teams, FDA Quality System Regulations, ISO 13485
• Type: other

Santa Clara

• Skills: procurement, construction contracts, nuclear quality assurance, vendor management, contract negotiation, market analysis, compliance, risk management, ERP platforms, NQA-1
• Type: other