cGMP Biotechnologist II - Upstream/Downstream Ops

ANTER CONSULTING PTE. LTD.; Singapore; On-site; SGD 52,000 - 90,000; Full time

Job summary

ANTER CONSULTING PTE. LTD. based in Tuas, Singapore, seeks a Biotechnologist II to perform cGMP manufacturing operations across upstream, downstream, or central services streams.

You will work with engineering and leadership on equipment setup, calibration, rework, and quality testing to ensure operational readiness. The role requires 1–3 years of hands-on experience in a cGMP biomanufacturing or pharmaceutical environment, with strong documentation and safety compliance skills.

Qualifications

• Education: Diploma or Bachelor's Degree in Biotechnology, Chemical Engineering, Biological Sciences, Pharmacy, or related field.
• Experience: 1–3 years in a cGMP biomanufacturing or pharmaceutical production environment.
• Technical: Familiarity with upstream/downstream unit operations and central services, plus cGMP and GDP knowledge.

Responsibilities

• Perform cGMP bioprocess operations across designated streams (upstream, downstream, or central services).
• Complete batch production records, logbooks, and documentation accurately and on time.
• Adhere to EHS, safety standards, and regulatory audits; support schedule execution and issue escalation.
• Assist with equipment setup, calibration, and plant maintenance during shifts; monitor inventory to reduce downtime.

Skills

Attention to detail

Documentation skills

cGMP awareness

Troubleshooting

Education

Diploma or Bachelor's Degree in Biotechnology / related field

Tools

Upstream/Downstream operations familiarity

Quality testing processes

Job description

ANTER CONSULTING PTE. LTD. based in Tuas, Singapore, seeks a Biotechnologist II to perform cGMP manufacturing operations across upstream, downstream, or central services streams.

You will work with engineering and leadership on equipment setup, calibration, rework, and quality testing to ensure operational readiness. The role requires 1–3 years of hands-on experience in a cGMP biomanufacturing or pharmaceutical environment, with strong documentation and safety compliance skills.