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