13 qa director jobs at 11 companies in Poway, CA

3w
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Director, Clinical QA
San Diego, California, United States
$182k-$248k/yr OnsiteFull Time
Neurocrine Biosciences
Neurocrine BiosciencesNASDAQ: NBIX: Develops pharmaceuticals for neurological, endocrine, and psychiatric disorders.
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, Quality Systems
San Diego, California, United States
$170k-$210k/yr OnsiteFull Time
Viking Therapeutics
Viking TherapeuticsNASDAQ: VKTX: Develops therapies for metabolic and endocrine disorders.
10+ YOE5+ MgmtBachelor's in life sciences or engineering, 10+ years QA experience with 5+ years in leadership; deep GMP/FDA/ICH knowledge, eQMS (Veeva) experience, QRM, audit and inspection readiness.
Veeva
2w
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Director, Quality Assurance - Technical
San Diego or United States
$189k-$246k/yr HybridFull Time
Travere Therapeutics
Travere TherapeuticsNASDAQ: TVTX: Developing and selling therapies for rare kidney diseases.
10+ YOEBachelor's in life science,10+ years FDA-regulated QA experience,experience managing teams,cGMP knowledge,validation and vendor oversight,MS Office proficiency,ability to travel 10-25%.
Microsoft Word, Microsoft Excel, Adobe, Microsoft PowerPoint
1mo
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Senior Director Quality Operations
Chaska or Carlsbad
$230k-$250k/yr OnsiteFull Time
Danaher
DanaherNYSE: DHR: Develops scientific instruments and diagnostic tools for healthcare markets.
10+ YOE6+ MgmtBachelor's in science/engineering (or Master's/Doctorate) with extensive executive experience (18–20+ yrs), 10+ years quality leadership in IVD/medical device, 6+ years people leadership, deep QA/QC/process validation and regulatory (FDA/ISO) knowledge.
Danaher Business System (DBS), Quality Management System (QMS)
1mo
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Associate Director, Development Quality Assurance
Carlsbad or Boston or Dublin or United States
$155k-$197k/yr HybridFull Time
Ionis Pharmaceuticals
Ionis PharmaceuticalsNASDAQ: IONS: Discovers and develops RNA-targeted medicines for serious diseases.
5+ YOEAdvanced degree and extensive GCP QA experience (varies by degree: BSc+12 yrs, MSc+8 yrs, PhD+5 yrs or equivalent). Strong knowledge of ICH/GCP, inspection readiness, audit conduct, CAPA management, risk-based QA, and ability to travel 30–40%.
3w
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Associate Director, Quality Assurance
San Diego or United States
$161k-$180k/yr HybridFull Time
Avenzo Therapeutics
Avenzo Therapeutics: Developing next-generation oncology therapies for cancer patients.
8+ YOE8+ years QA experience in life sciences, bachelor's in chemistry/biology required, experience with GMP/GCP/GLP, audits and inspections, electronic QMS (e.g., Veeva), strong communication and analytical skills, 15% travel.
Veeva, Microsoft Office, Microsoft SharePoint, Microsoft Teams
1mo
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Associate Director, Quality Operations
San Diego, California, United States
$160k-$230k/yr OnsiteFull Time
Codera
Codera: Provides end-to-end drug development services for biotechnology companies.
10+ YOE6+ MgmtDegree in a science discipline; 10+ years quality systems experience, 6+ years GxP service provision; vendor assessment, audit experience, QA/QC management, GxP operations knowledge, and ability to manage multiple workstreams.
2d
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Executive Director, GMP Quality Assurance
San Diego, California, United States
$270k-$290k/yr OnsiteFull Time
Artiva Biotherapeutics
Artiva BiotherapeuticsNASDAQ: ARTV: Develops allogeneic natural killer cell-based therapies for various diseases.
15+ YOE8+ Mgmt15+ years GMP QA experience in biologics/cell therapy with 8+ years senior quality leadership, bachelor's degree required, deep knowledge of 21 CFR/ICH regs, inspection and BLA experience.
3d
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Associate Director, Clinical Quality Assuranc
San Diego, California, United States
$175k-$195k/yr OnsiteFull Time
ADARx Pharmaceuticals
ADARx Pharmaceuticals: Develops RNA-targeting therapeutics for treating genetic and cardiometabolic diseases.
10+ YOE10+ years GCP QA experience in biotech/pharma, experience with late-stage trials and inspection readiness; bachelor's in life sciences/pharmacy required; advanced degree preferred; strong leadership and communication skills.
5d
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Sr/Exec Director, Quality Assurance GCP
San Diego or South San Francisco or United States
$250k-$290k/yr HybridFull Time
Erasca
ErascaNASDAQ: ERAS: Developing precision oncology medicines to treat cancer patients.
12+ YOE12+ years in GCP quality with regulatory inspection experience; demonstrated leadership in clinical QA, knowledge of ICH GCP and global regulations, ability to manage audits, CAPAs, and mentor staff.
1mo
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Senior Business Manager / Organizational & Sales Quality Assurance Director
San Diego, California, United States
$155k-$170k/yr HybridFull Time
SYNERGY HomeCare: Providing professional non-medical home care and companion services.
6+ YOE6+ MgmtMinimum 6 years experience in sales, quality assurance, or related roles; managing multinational research projects; developing sales strategies; establishing sales QA standards; budget and KPI management; leading large cross-functional teams; CRM and sales analytics experience.
CRM
2mo
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Associate Director/Director, Drug Safety & Pharmacovigilance (Quality & Compliance)
San Diego, California, United States
$180k-$230k/yr OnsiteFull Time
Arrowhead Pharmaceuticals
Arrowhead PharmaceuticalsNASDAQ: ARWR: Develops RNAi medicines to treat genetic and intractable diseases.
10+ YOE10+ years in pharmacovigilance with 9–10 years QA/compliance; BS in a related science; global PV regulatory knowledge; leadership and mentoring; audit/inspection experience; strong communication; PV software proficiency.
Pharmacovigilance databases, PV software
2w
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Associate Director, Quality Assurance - Technical
San Diego or United States
$150k-$195k/yr HybridFull Time
Travere Therapeutics
Travere TherapeuticsNASDAQ: TVTX: Developing and selling therapies for rare kidney diseases.
8+ YOEBachelors in life science,8+ years analytical experience in drug/biologics development with GMP QA and analytical validation expertise; knowledge of cGMP/ICH/FDA; ability to support audits and regulatory submissions; travel up to 10-20%.