CQV Engineer Biopharma Validation & Commissioning

A leading engineering consultancy in Singapore is seeking a Commissioning & Qualification Engineer to develop risk assessments and validation plans for bioprocess equipment and cleanroom systems. The ideal candidate will have 4-10 years of experience in validation and quality systems. Responsibilities include conducting tests, promoting GMP compliance, and preparing final reports. Candidates must possess strong communication skills and technical knowledge in utilities and systems validation.
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