GxP quality roles — QA, QC, compliance, audits, validation and quality systems in regulated manufacturing and clinical settings.
1,066 roles found · page 12 of 43
Baxter · Round Lake, IL
Abbott · Abbott Park, IL
Becton Dickinson · Irvine Laguna Canyon, CA
Danaher · Sunnyvale, CA
Neurocrine Biosciences · San Diego
Thermo Fisher Scientific · Bohemia, NY
Regeneron · Sleepy Hollow
Johnson & Johnson · New Brunswick, NJ
Sarepta Therapeutics · Andover, MA +1 more
AstraZeneca · Gaithersburg, MD
Regeneron · Rensselaer
PCI Pharma Services · Rockford, IL
Orthofix · Lewisville
Stryker · Kalamazoo, MI
Eurofins · Columbia, MO
LivaNova · Arvada, CO
Eurofins · Sunnyvale, CA
Thermo Fisher Scientific · Rockville, MD
Vir Biotechnology · San Francisco, CA
Thermo Fisher Scientific · Carlsbad, CA
Thermo Fisher Scientific · High Point, NC
Zimmer Biomet · San Diego, CA
Altasciences · Scranton, PA
Thermo Fisher Scientific · Greenville, NC
Thermo Fisher Scientific · Highland Heights, KY
Quality functions keep regulated work inspectable: maintaining the quality management system, running deviations and CAPAs, auditing suppliers and clinical sites, and hosting agency inspections. Postings usually signal which GxP applies — GMP for manufacturing, GCP for clinical, GLP for preclinical — and for device makers, ISO 13485 and 21 CFR Part 820. QC roles are typically lab-based and on-site by nature, while QA and compliance roles are more often hybrid.
Roles in this area are also listed as quality assurance jobs, GMP jobs, GCP auditor jobs, quality engineer jobs and validation jobs.
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