Director, GLP Quality Assurance — Oncology Biopharma

Scorpion Therapeutics; California (MO); On-site; USD 211,000 - 264,000; Full time

Job summary

Scorpion Therapeutics, a late-stage oncology biopharma developing RAS-targeted therapies, is seeking a Director of GLP Quality Assurance. This onsite role in Redwood City, CA leads GLP QA across internal and external labs supporting clinical studies.

The candidate will develop audit plans, manage vendor QA, and ensure regulatory adherence including 21 CFR Part 58 and ICH GCP. Required are a Bachelor’s or Master’s degree and 12+ years of global GLP QA experience with strong audit management.

Qualifications

• Bachelor’s or Master’s degree required.
• 12+ years of global GLP QA experience required.
• Extensive audit management skills required.

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

Skills

Audit management

Regulatory knowledge

GLP QA

Vendor management

Biomarker lab knowledge

Education

Bachelor’s or Master’s degree

Tools

Computerized systems validation

Job description

Scorpion Therapeutics, a late-stage oncology biopharma developing RAS-targeted therapies, is seeking a Director of GLP Quality Assurance. This onsite role in Redwood City, CA leads GLP QA across internal and external labs supporting clinical studies.

The candidate will develop audit plans, manage vendor QA, and ensure regulatory adherence including 21 CFR Part 58 and ICH GCP. Required are a Bachelor’s or Master’s degree and 12+ years of global GLP QA experience with strong audit management.