GxP quality roles — QA, QC, compliance, audits, validation and quality systems in regulated manufacturing and clinical settings.
260 roles found · page 1 of 11
Bristol Myers Squibb · Summit West - NJ - US
IQVIA · Durham, North Carolina, United States of America
Biogen · Research Triangle Park, NC
Regeneron · RENSS - TEMPEL LN
Gilead Sciences · United States - California - Foster City
Regeneron · RENSS - GLOBAL VIEW
Biogen · Research Triangle Park, NC
Regeneron · Limerick
Gilead Sciences · United States - California - La Verne
Agilent · 2 Locations
IQVIA · Reading, Berkshire, United Kingdom
Bristol Myers Squibb · Cruiserath - IE
Regeneron · Saratoga Springs
Bristol Myers Squibb · Cruiserath - IE
Amgen · US - Rhode Island - West Greenwich
IQVIA · Taguig City, Philippines
Gilead Sciences · Australia - Melbourne
Stryker · Carrigtwohill, Ireland
Gilead Sciences · Japan - Tokyo
Moderna
Bristol Myers Squibb · Cruiserath - IE
Edwards Lifesciences · USA - Utah – Salt Lake City
Gilead Sciences · United States - California - Foster City
Bristol Myers Squibb · Devens - MA
Stryker · Hamilton, Canada
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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