GxP quality roles — QA, QC, compliance, audits, validation and quality systems in regulated manufacturing and clinical settings.
1,066 roles found · page 32 of 43
Kiniksa Pharmaceuticals · Lexington, MA
Kiniksa Pharmaceuticals · Lexington, MA
Nurix Therapeutics · Brisbane, CA
Dyne Therapeutics · Waltham, MA
Dyne Therapeutics · Waltham, MA
Dyne Therapeutics · Waltham, MA
Kiniksa Pharmaceuticals · Lexington, MA
Inceptive · Palo Alto, CA
Sarepta Therapeutics · Bedford, MA
Vaxcyte · San Carlos, CA
Lyell Immunopharma · Bothell, WA
Vaxcyte · San Carlos, CA
Vaxcyte · San Carlos, CA
Vaxcyte · San Carlos, CA
Natera · San Carlos, CA
Tango Therapeutics · Boston, MA
Zifo
Danaher · Irvine, CA
Abbott · St. Paul, MN
PCI Pharma Services · GER
Haemonetics · Boston, MA
Merck · Elkhorn, NE
Abbott · Alameda, CA
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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