CQV Engineer: GMP Validation & Commissioning Expert

No deviation in Singapore is looking for a CQV Engineer to support commissioning, qualification, and validation activities in a pharmaceutical environment. You will be responsible for executing CQV documents, verifying stainless steel equipment, and collaborating with cross-functional teams to ensure compliance with GMP and GDP standards.

Ideal candidates should have a degree in Engineering or Life Sciences and 3 to 5 years of relevant experience, particularly with CIP/SIP systems. The company offers a comprehensive health policy and professional development opportunities.