Biotechnologist

Performs functions associated with GMP manufacturing operations within the biologics production facility, including working with engineers in set-up and calibration tasks, as well as performing rework and quality testing related to the production of parts, components and final materials.

Uses sophisticated programs (such as LIMS, SAP, automated control systems, etc.) to collect and evaluate operating data, which can be used to conduct on-line adjustments to products, instruments or equipment.

Determines and may assist in developing methods and procedures to control or modify the manufacturing process.

Commissioning & Qualification Engineer (CQV Engineer)

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 biotechnologist roles or commissioning engineering, preferrably from a bio-pharma environment.

Familiar with DeltaV operations

Able to work 12 hours rotating shift (day / night)

Contract role

Interested candidates please send in your updated resume in MS Word Format to:

••••@recruitexpress.com.sg

Subject: C&Q Engineer

EA Personnel: Kate Leau Wei Xuan (R1552331)

Company Registration No.: 99C4599