Associate Director, Quality Assurance - Computer System Validation
Hybrid Role - 3x per week in South San Francisco, CA
Meet has partnered with an exciting biotech that is looking for an Associate Director of QA, CSV to join their team! Our client has multiple late stage programs in cardiovascular and neuromuscular diseases. This position will be reporting into the Director of QA CSV.
Key Responsibilities
- You will be responsible for compliance oversight of CSV projects as an integral part of the QA team.
- You will provide leadership and oversight for GxP system implementations and updates.
- You will lead both contract and internal resources to support GxP CSV initiatives.
- You will participate in enterprise-wide GxP projects and contribute to a variety of cross-functional working groups.
Key Qualifications
- Minimum 8 years of relevant experience with 5+ specifically in pharma/biotech
- Strong experience working with Veeva Vault eTMF/eQMS, SAS, ERP, Trace Link
- Strong understanding of GCP, GMP, GLP practices
Please reach out to Ryan Moran to learn more about this opportunity:
✉: ryan.moran@meetlifesciences.com
