Job Description
Planet Pharma is seeking a CQV Specialist to lead re-validation within a GMP Drug Product program. You will define scope, frequencies, and requirements while coordinating quality, validation, and manufacturing teams to drive the project to completion. The role requires strong CQV expertise, 10+ years in Drug Product, and proven ability to drive validation strategies and cross-functional collaboration in a fast-paced setting. On-site Denmark contract opportunity with immediate start. #J-18808-Ljbffr
