San Francisco • 50 milesRemote · Hybrid · Onsite · Field · All Environments
San Francisco • 50 milesRemote · Hybrid · Onsite · Field · All Environments
San Francisco • 50 milesRemote · Hybrid · Onsite · Field · All Environments
San Francisco • 50 milesRemote · Hybrid · Onsite · Field · All Environments
472 fda jobs at 173 companies in San Francisco, CA
2d
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Healthcare & FDA Regulatory Law Specialist
San Francisco, California, United States
$100-$200/hr RemoteContract
3+ YOEJ.D. and U.S. bar admission required. Requires 3+ years of U.S. healthcare law, FDA regulatory, or healthcare compliance practice, with expertise in HIPAA, Anti-Kickback, Stark, False Claims Act, and FDA regulations.
ChatGPT, 510(k), PMA, NDA, CMS
2w
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FDA Laboratory Assistant full time Alameda, CA
Alameda, California, United States
OnsiteFull Time
High school diploma with science lab experience; ability to prepare media, decontaminate glassware, handle medical/pathological waste, follow USP/EPA/OSHA/FDA regulations; favorable background investigation (Tier 2/Public Trust) and US citizenship usually required.
5d
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Director, Marketing
San Mateo or San Francisco
$170k-$220k/yr HybridFull Time
10+ YOERequires 10+ years in FDA-regulated product marketing and commercialization, medical device or diagnostics experience, management experience, and a science or engineering bachelor's degree.
FDA
2d
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Director Supplier Quality
Pleasanton, California, United States
$172k-$344k/yr OnsiteFull Time
16+ YOEBachelor’s degree and 16 years of experience required, including 10 years in regulated environments; substantial FDA, ISO quality system, and medical device regulatory knowledge.
FDA, ISO, U.S. Code of Federal Regulations
3d
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SQF Coordinator
Fairfield, California, United States
$30-$33/hr OnsiteFull Time
Coordinates SQF certification, food safety programs, document control, HACCP and FDA compliance, audits, training, data review, and corrective actions in a food production facility.
SQF, FDA, HACCP, GMP, SOP
2mo
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Clinical Trial Manager
Campbell, California, United States
$136k-$152k/yr HybridFull Time
5+ YOE1+ Mgmt5+ years of clinical research management, preferably in medical devices; IDE studies; FDA/GCP knowledge; strong collaboration and communication; willingness to travel 20-30%
Clinical Data Management Systems, Regulatory Compliance, GCP, FDA Regulations, IDE
4d
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Sterilizer Operator I
San Jose, California, United States
$23-$25/hr OnsiteFull Time
High school diploma or related technical education; knowledge of QA/QC, document control, laboratory procedures, and FDA and ISO regulations. Strong organization and communication skills required.
FDA, ISO
2d
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Director Supplier Quality
Pleasanton, California, United States
$172k-$344k/yr OnsiteFull Time
16+ YOEBachelor's degree and 16 years of experience required, including 10 years in regulated environments; substantial FDA, ISO quality system, and U.S. medical device regulatory knowledge required.
FDA, ISO, U.S. Code of Federal Regulations
5d
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Specialist/Senior Specialist, Quality Assurance
Newark, California, United States
$130k-$160k/yr HybridFull Time
5+ YOEBachelor's degree in a scientific or related discipline; 5+ or 8+ years of biotech/pharmaceutical quality assurance experience; expertise in FDA, EU, and ICH regulations; strong organization and communication skills.
FDA, ICH
3mo
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Clinical Research Associate - VahatiCor
Santa Clara, California, United States
$99k-$133k/yr OnsiteFull Time
2+ YOEBachelor’s degree in life sciences; 2–4 years CRA medtech experience; FDA/ICH/GCP knowledge; strong communication; travel up to 50%; US work authorizatio
eCRF, TMF, SOPs, FDA regulations, ICH/GCP
2d
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VP of Clinical Science
San Francisco, California, United States
$260k-$320k/yr RemoteFull Time
MD, PhD, PharmD, or equivalent required; clinical strategy and evidence generation for a Class III PMA; trial design, biostatistics, GCP/FDA regulations, KOLs, publications, and startup leadership.
Artificial Intelligence, brain-computer interface, IDE, PMA, GCP, FDA
4d
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Associate Director, Preclinical Study Monitor and Operations
San Carlos, California, United States
$180k-$225k/yr OnsiteFull Time
10+ YOEBachelor's degree in life sciences, toxicology, pharmacology, or related field; 10+ years in drug discovery/development; knowledge of FDA, OECD, and GLP regulations; project management and communication skills.
FDA, OECD, Good Laboratory Practice (GLP), Master Service Agreements (MSAs), Statements of Work (SOWs)
1w
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VP Quality & Regulatory Affairs
Fremont, California, United States
$330k/yr OnsiteFull Time
15+ YOE8+ MgmtBachelor's degree in a scientific field or equivalent experience; 15+ years in senior regulatory and QA/QC roles, including 8+ years at executive level; FDA and international inspection leadership experience.
Quality Management System (QMS), CAPA, FDA, EMA, ICH, cGMP, GLP, GCP, 21 CFR Part 210, 21 CFR Part 211, 21 CFR Part 820, ISO 13485, EU MDR 2017/745
6d
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Analyst I, QC Environmental Monitoring
Hayward, California, United States
$68k-$94k/yr OnsiteFull Time
Bachelor's degree in life sciences preferred, laboratory equipment proficiency, computer literacy, data integrity knowledge, and familiarity with FDA, GLP, QSR, cGMP, GDP, EHS, SOPs, and regulated manufacturing.
BaxLIMS, Microsoft Office, FDA, GLP, QSR, cGMP, GDP, EHS, SOPs, CAPA, NCR, LIR, 6S, ESPP
5d
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Senior Specialist, Regulatory Programs (Part-Time)
Alameda, California, United States
$85-$95/hr OnsitePart Time
10+ YOEBachelor's degree preferred in science, 10+ years in compliance, quality, and CDMO/CMO management, 10+ years GMP/QA experience, and knowledge of FDA, EMA, ICH, and international biopharma regulations.
IND, NDA, BLA, FDA, EMA, ICH, GMP, CDMO, CMO, CRO
3d
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Senior Corporate Counsel, Global TechOps & Pharma Quality
South San Francisco, California, United States
$204k-$378k/yr OnsiteFull Time
7+ YOERequires 7+ years of US FDA/cGMP experience, a U.S. J.D., current good-standing admission to a U.S. state bar or California in-house eligibility, and strong legal communication skills.
FDA, Current Good Manufacturing Practices (cGMP), EMA
1w
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Sr Clinical Trials Manager
Foster City or United States
$158k-$204k/yr HybridFull Time
6+ YOEBA/BS with 6+ years or MA/MS with 4+ years of relevant clinical or life sciences experience; knowledge of FDA, EMA, ICH, and GCP requirements; clinical study leadership and mentoring experience.
FDA, EMA, ICH, GCP, Workday
1mo
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Senior Quality Engineer - Metals
Alameda, California, United States
$125k-$175k/yr OnsiteFull Time
5+ YOEBachelor's in engineering, 5+ years quality/manufacturing engineering in medical devices, knowledge of FDA QSR and ISO 13485, strong data analysis and problem-solving, experience with pFMEA, NCR/MRB/CAPA processes.
5 Why, Fishbone Diagram, Design of Experiments (DOE), regression analysis, pFMEA, Measurement System Analysis (MSA), FDA QSR, ISO 13485, NCR, MRB, CAPA
4d
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ISC Technician
Grove City or South San Francisco or Tokyo
OnsiteFull Time
Associate degree in electronics or equivalent experience; Microsoft Office proficiency, schematic and drawing interpretation, soldering, FDA-regulated medical device experience, quality systems knowledge, and strong communication and problem-solving skills.
Microsoft Office, FDA, ISO
4d
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Director Failure Investigation
Lodi or Sunnyvale
$160k-$220k/yr OnsiteFull Time
6+ YOE4+ MgmtBachelor's degree with 8+ years or master's/doctoral degree with 6+ years, including 4+ years managing people; regulated-industry, FDA/ISO, Lean Manufacturing, analytical, leadership, and communication experience required.
FDA, ISO, GMP, OSHA, CAPA, Lean Manufacturing, Lean Concepts
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