GxP quality roles — QA, QC, compliance, audits, validation and quality systems in regulated manufacturing and clinical settings.
260 roles found · page 8 of 11
LGC Group · London, England, gb
Source Bioscience · Nottingham, Nottingham Business Park, gb
Moderna
Zifo
Verve Therapeutics · New York, US
Zifo
Zifo
Zifo
Zifo
Cellares · Bridgewater, NJ
Illumina · India - Bengaluru - Manyata
Genesis Therapeutics · Paris
Illumina · Singapore - Woodlands - NorthTech
Cellares · Bridgewater, NJ
Cellares · Bridgewater, NJ
Verve Therapeutics · US - Remote
Erasca · San Diego, CA, South San Francisco, CA, or remote
Maravai LifeSciences · Jupiter, FL
Kiniksa Pharmaceuticals · Lexington, MA
Nurix Therapeutics · Brisbane, CA
Dyne Therapeutics · Waltham, MA
Genesis Therapeutics · Bay Area
Cellares · Bridgewater, NJ
AbCellera · Vancouver
Dyne Therapeutics · Waltham, MA
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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