Onsite Bioprocess Technician (cGMP) - Upstream/Downstream

Anter Consulting Pte. Ltd.; Singapore; In loco; SGD 56.000 - 89.000; Tempo pieno

Descrizione del lavoro

Anter Consulting Pte. Ltd. in Singapore seeks a Biotechnologist II to perform critical day-to-day functions in a cGMP biologics production facility. The role covers upstream, downstream, or central services, collaborating with engineering and leadership on equipment setup, calibration, and quality testing.

The successful candidate will ensure batch documentation is accurate, on schedule, and compliant with cGMP, safety, and quality standards in a cost-effective manner.

Competenze

• Diploma or Bachelor's degree in Biotechnology, Chemical Engineering, Biological Sciences, Pharmacy, or a related scientific discipline.
• 1–3 years of hands-on experience in a cGMP biomanufacturing or pharmaceutical production environment.
• Familiarity with upstream (cell culture/fermentation) or downstream (chromatography/filtration) unit operations, or central service operations (buffer/media prep).
• Good understanding of cGMP regulations, cleanroom protocol, and GDP (Good Documentation Practices).

Mansioni

• Perform routine bioprocess operations in compliance with cGMP guidelines and safety standards across designated processing streams.
• Assist engineers and technical staff with equipment set-up, routine calibration, troubleshooting, and plant maintenance/upkeep during assigned shift operations.
• Execute daily operational tasks assigned by the Lead Biotechnologist or Manufacturing Supervisor to maintain continuous operational readiness.
• Monitor and maintain localized inventory levels of consumables and raw materials to minimize downtime and waste.
• Ensure all individual training requirements remain current and fully completed.

Conoscenze

Upstream operations

Downstream operations

cGMP knowledge

Documentation practices

Formazione

Diploma or Bachelor's in Biotechnology/related field

Descrizione del lavoro

Anter Consulting Pte. Ltd. in Singapore seeks a Biotechnologist II to perform critical day-to-day functions in a cGMP biologics production facility. The role covers upstream, downstream, or central services, collaborating with engineering and leadership on equipment setup, calibration, and quality testing.

The successful candidate will ensure batch documentation is accurate, on schedule, and compliant with cGMP, safety, and quality standards in a cost-effective manner.