GxP quality roles — QA, QC, compliance, audits, validation and quality systems in regulated manufacturing and clinical settings.
260 roles found · page 4 of 11
Stryker · Cork, Ireland
Agilent · US-CO-Frederick
Agilent · 5 Locations
Amgen · Singapore Manufacturing - Tuas
Regeneron · RENSS - TECH VALLEY
Agilent · US-CO-Frederick
Edwards Lifesciences · USA - Utah – Salt Lake City
Bristol Myers Squibb · Devens - MA - US
Biogen · Cambridge, MA
Biogen · Cambridge, MA
Amgen · US - California - Thousand Oaks
Biogen · Research Triangle Park, NC
Agilent · 3 Locations
Edwards Lifesciences · USA - California – Irvine
Gilead Sciences · United States - California - La Verne
Regeneron · RENSS - TEMPEL LN
Medtronic · North Haven, Connecticut, United States of America
Biogen · Cambridge, MA
Amgen · US - California - Thousand Oaks
Regeneron · RENSS - TEMPEL LN
Gilead Sciences · United States - California - Foster City
Edwards Lifesciences · Singapore
IQVIA · Ithaca, New York, United States of America
Gilead Sciences · United States - California - Foster City
Gilead Sciences · 2 Locations
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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