Join a cutting-edge biotech company at the forefront of scientific innovation in the cancer space. We're seeking a Computer System Validation (CSV) Manager to lead and manage all validation activities across our GxP-regulated systems.
Key Responsibilities:
- Oversee CSV lifecycle for lab and manufacturing systems
- Ensure compliance with FDA, GAMP 5, and 21 CFR Part 11
- Collaborate with QA, IT, and system owners for audits and inspections
Qualifications:
- 5+ years in CSV within life sciences
- Strong understanding of GxP, data integrity, and regulatory requirements
- Excellent communication and project management skills