GLP QA Manager — On-Site Audits & FDA Readiness
Listed on 2026-10-18
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Quality Assurance - QA/QC
Regulatory Compliance Specialist, QA Specialist - Analyst/Manager
Crystal Bio Solutions seeks a hands-on Quality Assurance Manager to independently perform GLP QA activities at our Pleasanton, CA GLP bioanalytical laboratory. The role covers audits, master scheduling, and inspection readiness with senior management access.
This on-site position focuses on QA execution rather than people management. The candidate will host client audits, participate in FDA GLP inspections, and ensure strict adherence to FDA 21 CFR Part 58, SOPs, and CAPA processes while
Consider building your career as a GLP QA Manager — On-Site Audits & FDA Readiness at CRYSTAL PHARMATECH INC.
The position is based in Pleasanton, CA, United States.
This opportunity is part of our work in Finance, Bio & Pharmacology & Health.
The advertised compensation is 100..
We aim to respond to suitable candidates as soon as possible.
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