GxP quality roles — QA, QC, compliance, audits, validation and quality systems in regulated manufacturing and clinical settings.
260 roles found · page 7 of 11
Edwards Lifesciences · Singapore
Regeneron · Limerick
Regeneron · RENSS - TEMPEL LN
Bristol Myers Squibb · Summit West - NJ - US
Bristol Myers Squibb · Devens - MA - US
Regeneron · Hyderabad
Gilead Sciences · United States - California - Foster City
Agilent · 2 Locations
Biogen · Research Triangle Park, NC
Regeneron · RENSSELAER
Bristol Myers Squibb · Indianapolis - RayzeBio - IN
Edwards Lifesciences · USA - California – Irvine
Stryker · Portage, Michigan
Agilent · US-CO-Frederick
Biogen · Bangalore, India
Nurix Therapeutics · Brisbane, California
Kiniksa Pharmaceuticals · Lexington, MA
PTC Therapeutics · USA - New Jersey - Pennington
LGC Group · Manchester, NH, us
LGC Group · Bellshill, Scotland, gb
LGC Group · Berlin, BE, de
Moderna
Sarepta Therapeutics · 2 Locations
LGC Group · Berlin, BE, de
LGC Group · Lancashire, Bury, England, gb
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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