GMP CQV Validation Engineer – Equipment & Process Focus

Job Description

No deviation Pte. Ltd. is seeking a Validation Engineer to lead qualification and validation activities in a GMP pharma/biopharma manufacturing environment. You will plan, execute, document, and support validation for equipment, systems, utilities, and processes.

Key responsibilities include creating IQ/OQ/PQ protocols, reviewing test results, and supporting deviations, CAPA, and change control. Collaboration with Engineering, QA, and vendors is essential to success.

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NO DEVIATION PTE. LTD.

GMP CQV Validation Engineer – Equipment & Process Focus

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