Job Description

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
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-functional teams during the facility build-up phase
  • Supporting the establishment of robust quality and validation processes
Your ...

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