220 qa manager jobs at 169 companies in Westpark, CA
3w
Save
Mark Applied
Hide
QA Commercial Manager
Santa Ana, California, United States
$106k-$138k/yr OnsiteFull Time
5+ YOE2+ MgmtBS/BA preferred,5+ years QA experience in medical device/biopharma,2+ years people management,knowledge of FDA GMP/QSR,ISO 13485,IVDD/MDR,ACLS preferred,MS Office proficiency.
Microsoft Word, Microsoft Excel, Microsoft PowerPoint
6d
Save
Mark Applied
Hide
QA Manager
Pomona, California, United States
$123k-$149k/yr OnsiteFull Time
5+ YOE2+ MgmtRequires 5–7 years in regulated pharmaceutical quality assurance and control, 2–3 years of leadership, a scientific BSc, and knowledge of cGMP, quality systems, regulatory affairs, and stability protocols.
cGMP, QSR, GDP, CAPA, KPI
1mo
Save
Mark Applied
Hide
QA/QC Manager
Pasadena, California, United States
OnsiteFull Time
5+ YOE2+ MgmtBS in Chemistry or Engineering (MS preferred), 5+ years CGMP manufacturing experience, 2+ years supervisory experience, internal auditor training, ASQ certifications preferred, ISO 9001 and GMP proficiency, analytical lab experience, strong problem-solving and computer skills.
Microsoft Word, Microsoft Excel, Microsoft Access, Microsoft PowerPoint, SAP
2w
Save
Mark Applied
Hide
Project Inspector/ QA Manager- Travel Required
Augusta or Bakersfield or Birmingham or Boston or Cedar Rapids or Cincinnati or Columbus or Des Moines or Great Falls or Harrisburg or Jackson or Kansas City or Knoxville or Las Vegas or Little Rock or Los Angeles or Milwaukee or Oklahoma City or Pasco or Pittsburgh or Saint Louis or Santa Monica or Savannah or Wichita
$90k-$140k/yr FieldFull Time
5+ YOEBS preferred with 5+ years construction/project management experience, proven onsite supervisory experience, strong reporting skills, Microsoft Office proficiency, authorized to work in the U.S.
Microsoft Word, Microsoft Excel, Microsoft Outlook, Kahua
1mo
Save
Mark Applied
Hide
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
2w
Save
Mark Applied
Hide
Construction QA/QC Lead – Disaster Recovery
Los Angeles or Irvine or Riverside or California
$81k-$138k/yr RemoteFull Time
2+ YOEBachelor's in construction-related field or 3 years CDBG-DR construction experience,2+ years supporting CDBG-DR/CDBG-MIT,proficiency with Xactimate and Microsoft Excel,knowledge of building codes,team management and QA/QC skills.
Xactimate, Microsoft Excel
2w
Save
Mark Applied
Hide
QA Compliance Supervisor
Ontario, California, United States
$100k-$140k/yr OnsiteFull Time
1+ YOESupervisory QA role overseeing QMS, audits, CAPA, document control; bachelor's degree or 1-2 years related experience; strong Excel/Word skills; ISO13485 audit training preferred.
Microsoft Excel, Microsoft Word
2mo
Save
Mark Applied
Hide
QA/QC Specialist
Brea, California, United States
FieldFull Time
3+ YOE3+ years construction quality assurance/control or field inspection experience; bachelor's degree preferred; proficient in Microsoft Office, Procore, Bluebeam; strong communication, documentation, and problem-solving skills.
Microsoft Word, Microsoft Excel, Microsoft Outlook, Microsoft PowerPoint, Procore, Bluebeam
5d
Save
Mark Applied
Hide
QA/QC Supervisor
Commerce, California, United States
$65-$81/hr FieldFull Time
8+ YOE3+ MgmtRequires 8+ years of quality control experience, 3+ years supervising QA/QC, 5+ years as a CWI, ASME piping and welding expertise, and preferred SCWI/CWI or ICC certification. Associate degree or equivalent experience required.
Statistical Process Control (SPC), Microsoft Office, Google Workspace, Adobe, Bluebeam, Box
1mo
Save
Mark Applied
Hide
Manager, QA Method Validation
Carlsbad, California, United States
$114k-$212k/yr OnsiteFull Time
8+ YOEBachelor's in engineering/medical technology/biological sciences,8+ years clinical/GMP lab experience,3+ years supporting in vitro diagnostic development,knowledge of GxP/IVDR/ICH/ISO,statistical familiarity,strong communication.
3w
Save
Mark Applied
Hide
Senior Software QA Engineer
Irvine, California, United States
$107k-$140k/yr OnsiteFull Time
5+ YOE5+ years QA experience with automation leadership; test strategy, CI/CD, performance/security/accessibility testing; mentoring, strong communication and problem-solving; High School diploma required, Bachelor's preferred.
Playwright, Jenkins, Jira Software, Confluence, JMeter, Microsoft Office, Visio
3mo
Save
Mark Applied
Hide
Trainer-Coding & QA
San Bernardino, California, United States
$48-$65/hr OnsiteFull Time
3+ YOEBachelor's in Health Information Management preferred; minimum 3 years coding in acute care; CCS certification; strong knowledge of ICD/CPT; English communication and computer skills.
Word processing, Spreadsheets, Email, Presentation software, Coding systems
3mo
Save
Mark Applied
Hide
QA Specialist III
La Verne, California, United States
$107k-$139k/yr OnsiteFull Time
6+ YOE6+ years GMP experience with BS/BA; 4+ years with MS; pharmaceutical/biopharmaceutical background; GMP and Quality Systems knowledge; MES/LIMS/Web or document management familiarity; strong communication and Office skills.
SAP QM, MES, LIMS, GLIMS, document management systems
1mo
Save
Mark Applied
Hide
Manager/ Senior QA Associate, GxP Quality Systems
Carlsbad or Boston or Dublin
$71k-$102k/yr OnsiteFull Time
3+ YOEBachelor's degree in a science-related field, 3+ years quality assurance experience in pharmaceutical/biotech, strong knowledge of GxP/GMP and quality systems, familiarity with AI in GxP desirable, strong communication and problem-solving.
2mo
Save
Mark Applied
Hide
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
Save
Mark Applied
Hide
Lead QA Engineer
Los Angeles or Tustin or Dallas
$132k-$167k/yr HybridFull Time
5+ YOE2+ Mgmt5–8+ years software quality assurance, 2+ years in leadership; manual and automated testing; Selenium/Cypress/Playwright; API testing; CI/CD; Agile; Jira; programming in JavaScript/Python/Java.
Selenium, Cypress, Playwright, Postman, REST Assured, Jenkins, GitHub Actions, GitLab CI, Jira, JavaScript, Python, Java
1w
Save
Mark Applied
Hide
QA Lead – Robotics-Based Test Automation IRC299219
Lake Forest, California, United States
$145k-$155k/yr OnsiteFull Time
10+ YOEBS/MS or equivalent; onsite in Lake Forest, CA. 5+ years automation testing experience, 3+ years coordinator experience; hands-on with Ranorex and C#; Azure CI/CD, Visual Studio/Git; experience with regulated standards (IEC 62304, ISO 13485, 21 CFR 820) and AI-assisted tools.
Ranorex Automation Tool, C#, Visual Studio, Git, Azure CI/CD, GitHub Copilot, Claude
2w
Save
Mark Applied
Hide
Lead QA Automation Engineer
Glendale, California, United States
$155k-$195k/yr OnsiteFull Time
6+ YOE6+ years in quality/test engineering, experience building automated CI/CD test suites, production-grade test code, observability/monitoring, and mentoring junior engineers.
2mo
Save
Mark Applied
Hide
QA Lead
Santa Monica or Austin or Seattle
$70k-$90k/yr HybridFull Time
5+ YOE3+ Mgmt5+ years QA experience (3+ years as QA lead), experience with test strategy, automation, CI/CD, Jira, scripting (Python/JavaScript/C#), console and PC testing, familiarity with AI/ML-assisted tooling, and strong communication skills; high school diploma required.
Jira, Python, JavaScript, C#, Perforce, Unreal Engine, Unity, Microsoft Office, Copilot, Claude Code, Cursor, CI/CD, LLM
1mo
Save
Mark Applied
Hide
Manager, QA Method Validation
Carlsbad, California, United States
$114k-$212k/yr OnsiteFull Time
8+ YOEBachelor's in a related field, 8+ years in clinical/GMP labs, 3+ years supporting IVD development, regulatory knowledge (GxP, Part 11, ICH, ISO, CLIA/CAP, IVDR, QSR), molecular biology familiarity, statistical understanding, strong communication.
GxP, Part 11, ICH, ISO, CLIA/CAP, IVDR, QSR
Explore Jobs