Senior Director of GCP Quality Assurance

biophase • San Francisco Bay Area
Relocation
Apply
AI Summary

Biopharmaceutical organization seeking Senior Director of GCP Quality Assurance to provide strategic and operational oversight of clinical programs and external partners. Ensure compliance with ICH GCP and global regulatory requirements. Identify and mitigate compliance risks across programs.

Key Highlights
Provide GCP oversight to clinical teams and CROs/vendors
Lead risk-based GCP audits and oversee CAPA follow-up
Ensure clinical trials are conducted in accordance with regulatory requirements and best practices
Key Responsibilities
Provide GCP oversight to clinical teams and CROs/vendors
Lead risk-based GCP audits and oversee CAPA follow-up
Ensure clinical trials are conducted in accordance with regulatory requirements and best practices
Technical Skills Required
ICH GCP Global regulatory requirements
Benefits & Perks
Relocation assistance offered
Onsite 5 days a week - San Francisco, CA

Job Description


  • Relocation assistance is offered
  • Onsite 5 days a week - San Francisco , CA


Senior Director, GCP Quality Assurance

An established biopharmaceutical organization in the South San Francisco area is seeking an experienced Senior Director of GCP Quality Assurance to provide strategic and operational oversight of clinical programs and external partners. This on-site leadership role ensures compliance with ICH GCP and global regulatory requirements while maintaining high standards of data integrity and inspection readiness.


Key Responsibilities:

  • Provide GCP oversight to clinical teams and CROs/vendors.
  • Lead risk-based GCP audits (sites, CROs, vendors) and oversee CAPA follow-up.
  • Ensure clinical trials are conducted in accordance with regulatory requirements and best practices.
  • Identify and mitigate compliance risks across programs.
  • Support vendor oversight, quality metrics reporting, and continuous improvement initiatives.
  • Partner cross-functionally to implement fit-for-purpose quality systems and procedures.

Qualifications:

  • Bachelor’s degree in life sciences (advanced degree preferred).
  • 15+ years in biopharma QA, including progressive Clinical QA leadership.
  • 6+ years of direct GCP audit experience.
  • Strong knowledge of ICH GCP and global regulatory requirements.
  • Proven ability to assess compliance risk and drive practical, risk-based quality solutions.


Similar Jobs

Explore other opportunities that match your interests

Software Engineer, AI

Programming
•
5h ago

Premium Job

Sign up is free! Login or Sign up to view full details.

•••••• •••••• ••••••
Job Type ••••••
Experience Level ••••••

Coders Connect

San Francisco Bay Area

Founding Frontend Software Engineer

Programming
•
1d ago
Visa Sponsorship Relocation Remote
Job Type Full-time
Experience Level Not Applicable

Rec Gen

San Francisco Bay Area

Software Engineering Intern, Pokémon GO

Programming
•
3d ago

Premium Job

Sign up is free! Login or Sign up to view full details.

•••••• •••••• ••••••
Job Type ••••••
Experience Level ••••••

Scopely

San Francisco Bay Area

Subscribe our newsletter

New Things Will Always Update Regularly