GMP Qualification / Validation Engineers (m/f/d) – Singapore (Tuas)

We are currently looking for experienced GMP Qualification and Validation Engineers to support a large-scale pharmaceutical project in Singapore (Tuas).

This project involves the setup and commissioning of a new production facility, offering a unique opportunity to contribute from an early stage.

• Duration: Approx. 18 months

• Execution of equipment qualification and validation activities in accordance with GMP guidelines
• Support of commissioning activities for new production systems and equipment
• Planning and execution of temperature mapping studies
• Preparation and review of qualification documentation, including: IQ, OQ, PQ
• Ensuring compliance with regulatory requirements (e.g., EU GMP, FDA)
• Collaboration with cross-functional teams during the facility build-up phase
• Supporting the establishment of robust quality and validation processes