On-Site QA Consultant: Drug Product Manufacturing (3-Month Contract)

Planet Pharma is seeking a QA Consultant for Drug Product Manufacturing in Hillerød, Zealand Region. This role requires at least 5 years of Quality Assurance experience in the pharmaceutical industry, focusing on GMP compliance and quality records management.

The consultant will be responsible for reviewing deviations, CAPAs, and supporting compliance with regulatory requirements as part of a hands-on QA team. The role is full-time and on-site, offering the opportunity to work in a dynamic and fast-paced manufacturing environment.