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Director, GLP Quality Assurance
Job in
California, Moniteau County, Missouri, 65018, USA
Listed on 2026-09-14
Listing for:
Scorpion Therapeutics
Full Time
position Listed on 2026-09-14
Job specializations:
-
Quality Assurance - QA/QC
Regulatory Compliance Specialist
Job Description & How to Apply Below
Role
Director of GLP Quality Assurance at a late-stage oncology biopharma developing RAS-targeted therapies, responsible for ensuring GLP compliance across internal and external research labs supporting clinical studies.
Responsibilities- Develop audit plans
- Perform/vendor audits
- Review study protocols and reports for compliance
- Monitor vendor QA activities
- Manage regulatory adherence (e.g., 21 CFR Part 58, OECD, ICH GCP)
- Provide GLP training and SOP development
- Bachelor’s or Master’s degree
- 12+ years of global GLP QA experience
- Extensive audit management skills
- RQAP-GLP certification
- Strong regulatory knowledge
- Experience with bioanalytical, PK, biomarker labs, and computerized systems validation
Experience with testing facilities, bioanalytical labs, biorepositories, and AI/ML in biomarker labs; knowledge of US and EU GLP/GCP regulations.
CollaborationLiaises with vendors, internal nonclinical and clinical teams, and QA management.
Work SetupOnsite in Redwood City, CA.
Salary range $211K-$264K, competitive benefits, and development opportunities.
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