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.

Project Details

• Location: Tuas, Singapore
• Start: May / June (planned)
• Duration: Approx. 18 months

Your Responsibilities

• 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-function...