GxP quality roles — QA, QC, compliance, audits, validation and quality systems in regulated manufacturing and clinical settings.
260 roles found · page 6 of 11
Bristol Myers Squibb · Devens - MA - US
Regeneron · TARRYTOWN
Biogen · Baar, Switzerland
Edwards Lifesciences · 2 Locations
Edwards Lifesciences · Hong Kong-Kowloon
Bristol Myers Squibb · Hyderabad - TS - IN
Edwards Lifesciences · Ireland-Limerick
Stryker · Ventura, California
Gilead Sciences · United States - California - Foster City
Regeneron · Limerick
Biogen · Research Triangle Park, NC
Stryker · Belfast, United Kingdom
Regeneron · Limerick
Amgen · Singapore Manufacturing - Tuas
Amgen · US - Rhode Island - West Greenwich
Regeneron · Remote - United Kingdom
Gilead Sciences · United States - California - Foster City
Bristol Myers Squibb · Leiden – NL
Gilead Sciences · United States - California - La Verne
Bristol Myers Squibb · Bothell - WA - US
Gilead Sciences · United States - California - Foster City
Bristol Myers Squibb · Leiden – NL
Bristol Myers Squibb · Indianapolis - RayzeBio - IN
Regeneron · Dublin
Agilent · Canada-Prince Edward Island-Charlottetown
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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