1w
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Director, QA Engineering
Englewood Cliffs, New Jersey, United States
$180k-$200k/yr OnsiteFull Time
10+ YOE6+ Mgmt10+ years QA experience with 6+ years leading QA/SDET teams, expertise in test automation, CI/CD, cloud SDLC, and collaboration with engineering and product leadership.
Playwright, Cypress, Selenium
1mo
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Nuclear QA Director
Abilene, Texas, United States
HybridFull Time
10+ YOE10+ years in nuclear QA or related regulated quality roles; leads QA programs; strong audits, supplier quality, and documentation experience; BS in engineering/science or related field.
NQA-1, 10 CFR 50 Appendix B, ANs-15.8, DOE nuclear requirements, NRC licensing environments
1mo
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QA/QC Director
Glendale, California, United States
$100k-$200k/yr OnsiteFull Time
5+ YOE3+ Mgmt5+ years in pharmaceutical/biotech regulated industries, 3+ years QA/QC management, experience with CAPA, investigations, validation, audits, cGMP/GDP and ISO 9001 QMS, Bachelor's in a scientific discipline required.
ISO 9001-2015, Quality Management Systems (QMS), cGMP, GDP, CAPA
3d
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Director, Manufacturing QA
Waco, Texas, United States
$161k-$305k/yr HybridFull Time
15+ YOE6+ MgmtBachelor's in life science/pharmacy/engineering required; graduate degree preferred. 15+ years industry experience with ≥6 years management; manufacturing and QA experience; regulatory inspection experience; technical problem-solving and leadership skills.
3w
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Director, PV QA DSI
Basking Ridge, New Jersey, United States
$184k-$276k/yr OnsiteFull Time
10+ YOE10+ MgmtBachelor's degree required (Master's preferred), 10+ years PV QA or related experience, strong knowledge of GCP/GVP/regulatory guidance, REMS oversight experience preferred, leadership and communication skills.
2w
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Executive Director, CMC QA
Novato or South San Francisco
$294k-$363k/yr HybridFull Time
15+ YOE10+ Mgmt15+ years in regulated pharma/biotech with CMC QA experience, 10+ years leadership, bachelor’s in relevant field (advanced degree preferred), deep GMP and regulatory knowledge, inspection and supplier oversight experience.
Veeva, Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Teams, Microsoft Project
3mo
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GCP/GVP QA Director
Alameda, California, United States
$185k-$263k/yr OnsiteFull Time
13+ YOELeader for GCP/GVP QA systems, audits, and compliance; 13+ years pharma/biotech; strong regulatory and cross-functional collaboration.
GCP, GVP, Quality Management, Audits, CAPA, Regulatory Submissions, MS Office
1w
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Director, Clinical QA
San Diego, California, United States
$182k-$248k/yr OnsiteFull Time
10+ YOE12+ years industry experience (or 10+ with Master's) with GCP leadership, extensive audit/inspection experience, managerial background, and deep knowledge of FDA/ICH/EMA requirements.
1mo
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Director, CMC QA
Cambridge, Massachusetts, United States
$200k-$240k/yr HybridFull Time
10+ YOE10+ years cGMP QA in biotech/pharma; audits; vendor oversight; regulatory alignment; leadership in a small company.
1w
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Sr Director, QA- GxP Systems
Needham, Massachusetts, United States
$258k-$280k/yr HybridFull Time
10+ YOEBachelor's in life sciences,10+ years biotech/pharma QA with GxP systems, vendor oversight, CSV, audits, and Part 11 compliance; experience with eQMS/EDMS and regulated clinical workflows.
eQMS, EDMS
1w
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Associate Director, Clinical R&D QA US
Wilmington, Delaware, United States
OnsiteFull Time
5+ YOEBachelor's in science/healthcare,5+ years GCP QA experience with ≥5 years performing GCP audits,regulatory inspection experience,ability to travel up to 30%,strong communication and mentoring skills.
1mo
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Director, QA Operations (Quality Events and Data Analytics)
Tustin, California, United States
$166k-$207k/yr OnsiteFull Time
7+ YOEB.A./B.S. (life science) required, 7+ years pharma/biopharma experience, strong cGMP knowledge, QA leadership of deviations/CAPA/OOS/complaints, KPI development and analytics, people management, Microsoft Office proficiency.
Microsoft Excel, Microsoft Word, Microsoft PowerPoint
2mo
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Director, Commissioning QA/QC
Abilene or United States
$139k-$292k/yr OnsiteFull Time
12+ YOE5+ Mgmt12+ years leading commissioning/QAQC with 5+ years managing people; data center infra knowledge; startup sequencing, testing, energization, and turnover experience; Bachelor's or Master's in engineering/related fields plus experience; PMP/CxA/CCP/CQE/CMQ/OE and OSHA/LEED certifications preferred.
Budgeting Process and Management, Building Commissioning, Commissioning Processes, Control System Design, Data Center Infrastructure Construction, Data Center Operations, Electrical Systems, NFPA 70E, OSHA 10, OSHA Compliance, OSHA Regulations, OSHA Safety Assessments, Operational Activities, People Operations Function Management, Problem Solving, Project Management, Quality Control Analysis, Safety Procedures, Stakeholder Management, Technical Program Management, Testing, Troubleshooting, Vendor Management
2w
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Associate Director, GMP QA Operations
Waltham, Massachusetts, United States
$160k-$195k/yr OnsiteFull Time
8+ YOEBachelor's in engineering/science (Master's preferred), 8+ years in cGMP environment and 5+ years in QA, experience overseeing CMOs/CDMOs, knowledge of FDA/EMA regulations, GxP QA systems, strong communication and decision-making skills.
Microsoft Office, SmartSheet, Veeva
1mo
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Associate Director, QA Computer System Validation
Radnor, Pennsylvania, United States
$185k-$215k/yr HybridFull Time
10+ YOEBachelor’s degree in engineering or science; 10+ years QA/CSV experience; knowledge of GxP, CFR 21 Part 11, EMA/FDA; vendor audits; leadership.
Veeva Vault eQMS, Veeva eTMF, CTMS, Medidata Rave, SAS, TraceLink, Oracle Fusion
3w
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Director of Software QA
Kirkland, Washington, United States
HybridFull Time
7+ YOE7+ years leading Java-based test automation for web applications; hands-on Java; API automation (SoapUI/Rest Assured), Selenium, Cucumber/Gherkin, Eclipse/IntelliJ, Postman; Agile/DevOps; AWS and MongoDB/MySQL a plus; bachelor's preferred.
Java, SoapUI, Rest Assured, Selenium, Cucumber, Gherkin, Eclipse, IntelliJ, Postman, GitHub Copilot, Cursor, Claude, AWS, MongoDB, MySQL
2mo
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Executive Director, GCP QA (Good Clinical Practice, Quality Assurance)
Redwood City, California, United States
$265k-$331k/yr OnsiteFull Time
15+ YOE10+ Mgmt15+ years in pharma/biotech; 10+ years in GCP QA or clinical quality leadership; advanced life sciences degree; oncology regulatory experience; leading regulatory inspections; strong leadership and communication.
GCP QA, RBQM, GxP, TMF, CAPA
1mo
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Sr. Director, RA/QA Strategy & Business Integration
United States
$231k-$289k/yr RemoteFull Time
12+ YOE5+ MgmtBachelor's in life sciences/engineering, 12+ years RA/QA experience in biotech/diagnostics/devices, 5+ years leadership, experience with FDA/CLIA/CAP/IVDR, stakeholder influence, external engagement, and knowledge of HIPAA.
1w
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Associate Director, GCP/GLP/GVP QA
Boston, Massachusetts, United States
$160k-$240k/yr HybridFull Time
8+ YOE8+ years industry experience with 5+ years GCP QA or clinical trial QA, experience with GCP/GLP/GVP regulations and regulatory inspections, strong communication and project management skills.
4d
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IT Director (QA)
Sacramento County or Vacaville or California
$9k-$13k/mo RemoteFull Time
Lead statewide QA policy and team, implement automation, ensure testing and reliability, collaborate with DevOps/Development/operations, provide strategic QA leadership; must reside in California and meet class specification.
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