17 qa director jobs at 15 companies in Camden, NJ
3w
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Associate QA Director
Durham or Indianapolis or Wayne
$89k-$247k/yr OnsiteFull Time
10+ YOE10+ years GxP quality assurance experience in pharmaceutical/technical settings, audit experience, strong problem solving, risk analysis, communication and leadership skills.
2d
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Director, QA Operations
Ireland or South San Francisco or Radnor
€122k-€163k/yr HybridFull Time
10+ YOEBachelor's degree preferred; 10+ years in pharmaceutical manufacturing, team leadership, regulatory inspections or audits, global GMP regulations, MS Office, communication, organization, and independent decision-making.
Microsoft Office
1mo
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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.
6d
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Sr. Director/Executive Director, R&D/Clinical QA
Monmouth Junction, New Jersey, United States
$235k-$275k/yr HybridFull Time
12+ YOE8+ MgmtBachelor's degree in science or related field; 12–15 years of pharmaceutical or biotechnology quality experience, including 8–10 years of R&D or clinical QA leadership. Requires GxP, audit, inspection, and regulatory expertise.
Quality Management System (QMS), SOPs, CAPA, FDA, ICH Guidelines, EU Clinical Trial Regulation, EMA, MHRA, PMDA, GCP, GVP, GLP, GxP, ALCOA++, ALCOA+, clinical trial systems and technologies
2d
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Associate Director, Clinical QA
Princeton or Redmond
$150k-$190k/yr HybridFull Time
8+ YOEBachelor's degree in a relevant life sciences field, 8+ years in clinical quality or related pharmaceutical functions, and 5+ years of direct GCP quality assurance experience with audits and inspections.
Clinical Quality Management System (QMS), Risk-Based Quality Management (RBQM), Quality Tolerance Limits (QTLs), Standard Operating Procedures (SOPs)
2mo
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Director, GPV Compliance & Business Management (QA)
Princeton, New Jersey, United States
$186k-$279k/yr OnsiteFull Time
6+ YOEBachelor's degree required; minimum 6 years PV compliance or quality management experience; experience with GxP/GVP/GCP inspections, vendor oversight, global settings, CAPA/deviation management, audit readiness, and Microsoft Office proficiency.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint, Microsoft Outlook
2d
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Director, Quality (External Manufacturing)
King of Prussia, Pennsylvania, United States
HybridFull Time
15+ YOEBachelor's degree in chemistry, biology, or related field; 15+ years in pharmaceutical manufacturing, technical operations, or QA, including 12+ years of direct QA experience; strong cGMP and regulatory expertise.
Microsoft Office, Veeva
1mo
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Director, Quality
Princeton, New Jersey, United States
$190k-$230k/yr OnsiteFull Time
Bachelor's in chemistry/engineering/natural sciences,10+ years pharmaceutical experience with leadership,extensive QA/QC knowledge,cGMP and ICH familiarity,ability to manage audits,inspections,and batch disposition.
3mo
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Director, Quality Engineering
New York or Philadelphia or Atlanta
OnsiteFull Time
10+ YOE5+ Mgmt10+ years QA in software, 5+ years leadership; QE in P&C insurance; automation and SDLC experience; hands-on tools like Selenium/Cypress; strong leadership.
Selenium, Cypress, Tosca, LoadRunner, Postman, CI/CD, Cloud
1d
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Director of IT Engineering
Whitemarsh Township, Pennsylvania, United States
HybridFull Time
10+ YOE5+ MgmtBachelor's or master's degree preferred in IT, business, or related field; 10+ years application or integration engineering, 5+ years management, ERP, integration architecture, API, ETL, CRM, vendor, Agile, and Scrum experience.
Dell Boomi, API, Azure, ETL, CRM, Claude Code, ChatGPT, ERP, Agile, Scrum, CI/CD, QA
1mo
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Associate Director, Quality Assurance
Pennsauken, New Jersey, United States
$110k-$114k/yr OnsiteFull Time
5+ YOEBachelor's degree required, RN preferred; 5+ years related experience with prior supervisory experience; strong writing and presentation skills; Microsoft Excel/Word/PowerPoint proficiency; ability to travel for QA activities.
Microsoft Excel, Microsoft Word, Microsoft PowerPoint
2w
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Senior Director, Clinical Supply Release
Conshohocken, Pennsylvania, United States
$245k-$299k/yr OnsiteFull Time
15+ YOEBS in science/engineering,15+ years GMP QA/release experience with clinical supply,strong documentation and cross-functional coordination,inspection readiness,ability to travel 20-30% domestic and international.
Veeva Vault Quality (eQMS)
1w
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Medical Director/Senior Medical Leader - Oncology Late Development - Prostate
Spring House, Pennsylvania, United States
$199k-$344k/yr HybridFull Time
3+ YOEAdvanced medical degree, postdoctoral fellowship, and 3+ years of relevant urology or oncology clinical research experience; board-certified or board-eligible uro-oncologist or oncologist preferred.
Electronic Case Report Forms (eCRFs), Data Management, Biostatistics, Regulatory, Quality Management, Quality Assurance, Clinical Research Organization (CRO), NDA, MAA
2w
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Director of Abatement, Office of Environmental Services
Philadelphia, Pennsylvania, United States
$93k-$122k/yr OnsiteFull Time
9+ YOE4+ MgmtLeads planning and oversight of asbestos, lead, and other environmental programs; requires bachelor\u0002s degree, nine years professional environmental compliance experience (four supervisory), PA licenses and ability to manage contracts and QA/QC.
2mo
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Associate Director, Quality Change Management
Conshohocken, Pennsylvania, United States
$164k-$201k/yr OnsiteFull Time
10+ YOEBS in science/engineering required, 10+ years GMP QA/QMS with change control leadership, eQMS (Veeva Vault) experience preferred, cross-functional governance and inspection-readiness expertise.
Veeva Vault Quality (eQMS)
2w
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Associate Director, Quality Assurance (Clinical Research Preferred)
Durham or Indianapolis or Wayne
$89k-$247k/yr RemoteFull Time
10+ YOE10+ years QA experience in pharmaceutical/biotech/CRO/clinical research, strong GxP/GCP knowledge, audit and CAPA experience, leadership, risk assessment, and Microsoft Office proficiency.
Microsoft Office
6d
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Director of Cranbury GMP Compliance (5606)
Cranbury, New Jersey, United States
$134k-$229k/yr OnsiteFull Time
12+ YOE5+ MgmtBS, MS, or PhD in a relevant scientific or engineering discipline; 12+ years in biologics, pharmaceutical manufacturing, QC, CMC, or technical operations; 5+ years of leadership or management experience.
GMP, QC, Engineering, QA, MSAT, Validation, PPQ, CMC, CROs, CDMOs, PLI, PAI
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