Validation Engineer

Are you a CIP expert? Do you have experience working in the pharmaceutical industry? Are you looking for a new role?

We are currently supporting a global biopharmaceutical client in Denmark looking for a highly experienced CIP Validation Engineer to join their project team. This role focuses on clean-in-place (CIP) systems, with responsibilities spanning design input, commissioning & qualification (CQV), and operational troubleshooting post-startup. This position is ideal for a candidate with deep technical understanding of CIP processes and systems, a background in GMP manufacturing, and the ability to work cross-functionally with design, engineering, and operations teams.

Experience:

• Minimum 5–10 years of hands-on CIP validation experience in GMP-regulated environments (biotech/pharma).
• Proven track record in CQV lifecycle execution for CIP systems (design input, SAT, FAT, IQ/OQ/PQ).
• Strong understanding of CIP principles, automated cleaning sequences, and critical cleaning parameters.
• Experience supporting investigations, deviations, and operational troubleshooting.
• Comfortable working with cross-functional teams including operations, QA, automation, and vendors.
• Fluent in English; knowledge of Danish is a plus but not required.

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