GxP quality roles — QA, QC, compliance, audits, validation and quality systems in regulated manufacturing and clinical settings.
1,066 roles found · page 7 of 43
Gilead Sciences · Foster City, CA
ICON · Farmingdale, NY
Becton Dickinson · Covington BMD, GA
QIAGEN · Beverly
Eurofins · Lancaster, PA
Thermo Fisher Scientific · Boston, MA
Thermo Fisher Scientific · New Brunswick, NJ
Thermo Fisher Scientific · Santa Clara, CA
Thermo Fisher Scientific · Allentown, PA
Eurofins · San Jose, CA
Thermo Fisher Scientific · Logan, UT
AbbVie · North Chicago, IL
Eurofins · Columbia, MO
Danaher · Austin, TX
AbbVie · North Chicago, IL
Eurofins · Sanford, NC
Catalent · Kansas City, MO
Cencora · Carrollton, TX
Eurofins · Sanford, NC
iRhythm Technologies · San Francisco, CA
Edwards Lifesciences · Irvine, CA
Thermo Fisher Scientific · Middletown, VA
Merck · West Point, PA
Merck · Durham (old Oxford), NC
Eurofins · Sanford, NC
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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