Are you a Validation Engineer with hands-on experience with cleaning validation activities within a downstream manufacturing environment?

We are currently supporting a large pharmaceutical organisation in Denmark seeking a Validation Engineer to join their team. This role will focus on cleaning validation activities within a downstream manufacturing environment, supporting ongoing deviations, PPQ campaigns, and documentation through KNEAT.

Some of the skills the Validation Engineers are required to possess experience with are:

• Hands-on experience in Cleaning Validation (essential).
• Experience working with KNEAT for validation documentation.
• Previous involvement in downstream bioprocessing environments
• Solid understanding of GMP regulations and validation lifecycle principles.
• Fluent in English (written and verbal).

This is a fantastic opportunity to join a large pharmaceutical company in Denmark– feel free to share your CV for immediate consideration