GxP quality roles — QA, QC, compliance, audits, validation and quality systems in regulated manufacturing and clinical settings.
260 roles found · page 3 of 11
Gilead Sciences · United States - California - La Verne
Regeneron · Limerick
Amgen · US - Rhode Island - West Greenwich
Agilent · China-Shanghai
IQVIA · 9 Locations
Gilead Sciences · Japan - Tokyo
Gilead Sciences · Ireland - Cork
Stryker · Gurugram, India
Regeneron · RENSS - GLOBAL VIEW
Edwards Lifesciences · USA - Utah – Salt Lake City
Gilead Sciences · 2 Locations
Bristol Myers Squibb · Devens - MA - US
Amgen · US - Rhode Island - West Greenwich
Regeneron · Hyderabad
Bristol Myers Squibb · Bothell - WA - US
Agilent · US-CA-Santa Clara
Bristol Myers Squibb · Devens - MA - US
Edwards Lifesciences · USA - Utah – Salt Lake City
Regeneron · RENSSELAER
Regeneron · Limerick
Regeneron · Limerick
Edwards Lifesciences · USA - California – Irvine
Edwards Lifesciences · USA - California – Irvine
Bristol Myers Squibb · Leiden – NL
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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