Job Description
Manage end-to-end equipment lifecycle processes, from design specifications to operational readiness Ensure pharmaceutical and biologics manufacturing facilities and utilities meet strict cGMP regulations. Protocol Execution: Generating and executing C&Q protocols (FAT/SAT, IQ, OQ, VMP) for process systems, utilities, and lab equipment. Compliance & Validation: Ensuring systems meet cGMP and regulatory authority requirements. Troubleshooting: Investigating deviations and executing root-cause analyses for malfunctioning manufacturing systems (Delta V). Contractor Management: Supervising and guiding external vendors, contractors, and junior engineering staff. Requirements: Min. Degree in any relevant science field Possess prior working experience in biotechnology or project engineering, preferrably from a bio-pharma environment. Familiar with DeltaV operations Able to work 12 hours rotating shift (day / night) Interested candidates, please forward your resume to Consultant: Jalene Tan (R26160390) Recruit Express Pte Ltd (99C4599) jalenetan@recruitexpress.com.sgNo.: R26160390
