GMP CQV Validation Engineer – Equipment & Process Focus

NO DEVIATION PTE. LTD.

Singapore

On-site

SGD 60,000 - 90,000

Full time

8 days ago

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Job summary

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.

Qualifications

Bachelor's or higher in Engineering, Pharmaceutical Sciences, Biotechnology or Life Sciences.
Experience in validation, CQV, or pharmaceutical manufacturing.
Familiarity with GMP, IQ/OQ/PQ protocols and data integrity principles.

Responsibilities

Prepare and execute validation documentation (IQ/OQ/PQ plans, protocols, reports).
Plan and perform qualification for equipment, utilities, and processes.
Coordinate deviations, CAPA, and change controls.
Ensure traceability and data integrity per ALCOA+.
Collaborate with Engineering, QA, QC, and vendors.
Support regulatory inspections and audits.