GxP quality roles — QA, QC, compliance, audits, validation and quality systems in regulated manufacturing and clinical settings.
260 roles found · page 10 of 11
Lyell Immunopharma · Bothell, Washington, United States
LGC Group · Berlin, BE, de
Zifo
Cogent Biosciences · Remote, United States
Vaxcyte · Visp, Valais, Switzerland
Vaxcyte · US - Remote
Biocytogen
Lyell Immunopharma · Bothell, Washington, United States
Insitro · South San Francisco, CA
Zifo
LGC Group · Berlin, BE, de
Vaxcyte · San Carlos, California, United States
Vaxcyte · San Carlos, California, United States
Vaxcyte · San Carlos, California, United States
LGC Group · Berlin, BE, de
Iovance Biotherapeutics · Phildelphia
Lyell Immunopharma · Bothell, Washington, United States
Lyell Immunopharma · Bothell, Washington, United States
Orchard Therapeutics
Zifo
BridgeBio Pharma · Remote - USA
LGC Group · Berlin, BE, de
Vaxcyte · San Carlos, California, United States
Tango Therapeutics · Boston, MA
Zifo
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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