51 quality director jobs at 40 companies in La Mesa, CA
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Acoustics Quality Director
Northridge or Tijuana or Dandong
$173k-$254k/yr RemoteFull Time
15+ YOEBachelor's in engineering required (Master's preferred); 15+ years in quality/engineering/operations in acoustics or precision manufacturing; multi-site leadership; QMS/ISO9001 experience; NVH, reliability, and advanced problem-solving skills; willingness to travel 15-20% and complete background/drug screen.
Power BI, Minitab, CRM, Windchill, SAP
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Acoustics Quality Director
Northridge or Tijuana or Dandong
$173k-$254k/yr HybridFull Time
15+ YOESenior quality leader for acoustics products with 15+ years in quality/engineering/operations, bachelor’s in engineering required, ISO 9001/QMS experience, multi-site leadership, NVH/acoustic testing expertise, travel 15-20%.
Quality Management System (QMS), ISO 9001, FMEA, DOE, SPC, Kaizen, DMAIC, Power BI, Minitab, CRM, Windchill, SAP
2w
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Senior Director, Quality
San Diego, California, United States
$225k-$260k/yr OnsiteFull Time
12+ YOE5+ MgmtBS in a scientific discipline,12+ years pharma/biotech quality experience with biologics/cellular therapy,5+ years management,experience with FDA/ICH/GxP,inspection hosting,project planning,and Microsoft Office proficiency.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint
1w
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Director - Quality
Oceanside, California, United States
$168k-$180k/yr OnsiteFull Time
5+ YOE5+ MgmtBachelor's degree in engineering or quality field, 5+ years progressive senior quality management experience, ISO/IATF audits, Six Sigma/Lean/Kaizen experience, ERP usage, ASQ-Certified Quality Engineer, IATF 16949 and Black Belt certifications, fluent Spanish.
ISO 9001, IATF 16949, ERP
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Senior Director Quality Operations
Chaska or Carlsbad
$230k-$250k/yr OnsiteFull Time
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)
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Director of Product Quality
San Diego, California, United States
$200k-$240k/yr OnsiteFull Time
15+ YOE10+ MgmtBachelor's degree required (engineering preferred). 15+ years relevant quality engineering/control experience, 10+ years supervisory experience. ASQ Quality Engineer required; Six Sigma Black Belt preferred. Deep ISO/FDA, CAPA, validation, DOE, and statistical analysis expertise.
1w
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Quality Control Director
Carlsbad, California, United States
$195k-$205k/yr OnsiteFull Time
10+ YOE10+ MgmtBachelor's, master's, or Ph.D. in life science; 10+ years of leadership experience in medical device or pharmaceutical industries; FDA-regulated audit, GMP, ISO, validation, CAPA, and team leadership experience.
SOPs, ISO 13485, ISO 14971, GMP, GLP, QSR, ICH Q1A, ICH Q2, 21 CFR 820.30, CAPA, FDA
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Director, Quality Systems
San Diego, California, United States
$170k-$210k/yr OnsiteFull Time
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
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Sr. Director Quality Systems
San Diego, California, United States
$220k-$353k/yr OnsiteFull Time
12+ YOELead MMS quality systems across San Diego and Tijuana; drive QMS harmonization and regulatory compliance (FDA QSR, ISO 13485, EU MDR); collaborate with MMS leaders and regulators; travel as needed.
Trackwise, Agile, Documentum
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Associate Director, Quality Operations
San Diego, California, United States
$160k-$230k/yr OnsiteFull Time
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.
4w
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Director, Quality Assurance - Technical
San Diego or United States
$189k-$246k/yr HybridFull Time
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
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Director, Quality & Regulatory- Mergers & Acquisitions (M&A)
Colorado Springs or Nashville or Bothell or Gainesville or San Diego or Plymouth or Cambridge
$162k-$258k/yr HybridFull Time
15+ YOE15+ years in FDA-regulated medical device environments, leadership in quality/regulatory and M&A, Bachelor's required (Master's/MBA preferred), knowledge of FDA/ISO/EU MDR, QMS and KPI-driven governance.
QMS, FDA, ISO 13485, ISO 14971, EU MDR, TSLA, KPI
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Associate Director, Quality Assurance
San Diego or United States
$161k-$180k/yr HybridFull Time
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
2mo
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Associate Director, Development Quality Assurance
Carlsbad or Boston or Dublin or United States
$155k-$197k/yr HybridFull Time
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%.
1d
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Managing Director, Quality Intelligence & Causal Analysis
New York or Los Angeles or Troy or Houston or Chicago or Grand Rapids or Owings Mills or Columbia or Richmond or Memphis or Raleigh or Boston or San Jose or San Francisco or Austin or Kalamazoo or Spokane or Denver or Atlanta or Orlando or Dallas or Phoenix or San Antonio or Milwaukee or Madison or McLean or Melville or Woodbridge or Stamford or Miami or Philadelphia or Charlotte or Greenville or West Palm Beach or Costa Mesa or St. Louis or Fort Lauderdale or Seattle or Pittsburgh or Tulsa or Cincinnati or Cleveland or Columbus or Akron or Tampa or Minneapolis or Salt Lake City or Norfolk or Jacksonville or Nashville or Las Vegas or Indianapolis or San Diego or Metairie or Tallahassee or Omaha
$240k-$280k/yr OnsiteFull Time
10+ YOEBachelor's degree in accounting, economics, or data analytics; CPA required; 10+ years in accounting, audit quality, risk, regulatory, or analytical work; advanced Excel skills and leadership experience.
Microsoft Excel, Microsoft Office Suite, Microsoft Word, Microsoft PowerPoint, Microsoft Outlook
2mo
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Director Quality Improvement & Population
San Marcos or San Diego County or Riverside County
$121k-$187k/yr OnsiteFull Time
5+ YOEBachelor's in nursing and 5+ years clinical nursing experience required; experience leading quality improvement and population health programs; familiarity with risk stratification, regulatory standards (PCMH, CMS, NCQA, HRSA), data analytics, staff development; MPH and Lean/Six Sigma preferred.
1mo
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Director, External Quality Assurance (GMP)
Pasadena or San Diego
$198k-$236k/yr HybridFull Time
12+ YOEBachelor's in a scientific discipline and minimum 12 years GMP Quality/CMC experience with extensive CMO oversight; strong leadership, vendor management, regulatory knowledge, document authorship, and relationship-management skills.
2w
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Executive Director, GMP Quality Assurance
San Diego, California, United States
$270k-$290k/yr OnsiteFull Time
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.
1mo
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Director, External Quality Assurance (GMP)
Pasadena or San Diego
$198k-$236k/yr HybridFull Time
12+ YOEBachelor's degree in a scientific discipline and 12+ years of GMP Quality/CMC experience with extensive CMO oversight; experience in GxP/GMP, vendor management, document control, CAPA/change control, root cause analysis, leadership and cross-functional collaboration.
2mo
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Director, QC
San Diego, California, United States
$151k-$170k/yr OnsiteFull Time
12+ YOE6+ MgmtBachelor's in life sciences required; 12+ years QC experience in GMP pharmaceutical/CDMO environments, 6+ years leadership experience. Strong cGMP knowledge, electronic laboratory systems (LIMS/CDS/SDMS/ELN), Microsoft Office, and analytical/statistical skills (JMP preferred).
LIMS, CDS, SDMS, ELN, Microsoft Office, JMP
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