GxP quality roles — QA, QC, compliance, audits, validation and quality systems in regulated manufacturing and clinical settings.
260 roles found · page 9 of 11
Dyne Therapeutics · Waltham, MA
Maravai LifeSciences · San Diego, CA
Dyne Therapeutics · Waltham, MA
LGC Group · Tipperary, IRELAND, ie
Dyne Therapeutics · Waltham, MA
Kiniksa Pharmaceuticals · Lexington, MA
Cellares · South San Francisco, CA
Dyne Therapeutics · Waltham, MA
Cellares · Bridgewater, NJ
Cellares · Bridgewater, NJ
Healx · Cambridge
Inceptive · Palo Alto, CA
Zifo
Sarepta Therapeutics · Andover, MA
LGC Group · Luckenwalde, BB, de
Illumina · US - California - San Diego
Illumina · India - Bengaluru - Manyata
Illumina · India - Bengaluru - Manyata
Illumina · India - Bengaluru - Manyata
Sarepta Therapeutics · Bedford, MA
Illumina · US - California - San Diego
Illumina · India - Bengaluru - Manyata
Vaxcyte · San Carlos, California, United States
LGC Group · Berlin, BE, de
Biomapas
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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