GxP quality roles — QA, QC, compliance, audits, validation and quality systems in regulated manufacturing and clinical settings.
260 roles found · page 5 of 11
Edwards Lifesciences · USA - California – Irvine
Regeneron · Hyderabad
Bristol Myers Squibb · Devens - MA - US
Bristol Myers Squibb · Leiden – NL
Regeneron · RENSS - TECH VALLEY
Stryker · Limerick, Ireland
Agilent · US-CO-Boulder
Bristol Myers Squibb · Devens - MA - US
Amgen · US - Puerto Rico - Juncos
Gilead Sciences · United States - California - Foster City
Bristol Myers Squibb · 4 Locations
Stryker · Cary, Illinois
Regeneron · Limerick
Edwards Lifesciences · Malaysia-Kuala Lumpur BSC
Amgen · Netherlands - Breda
Stryker · Flower Mound, Texas
Bristol Myers Squibb · Indianapolis - RayzeBio - IN
Edwards Lifesciences · USA - California – Irvine
Amgen · India - Hyderabad
Regeneron · RENSSELAER
Regeneron · Remote - United States
Gilead Sciences · United States - California - Foster City
Bristol Myers Squibb · Bothell - WA - US
Agilent · US-CA-Santa Clara
Gilead Sciences · United States - California - Foster City
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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