Biotechnologist

ORION PROJECT SERVICES PTE. LTD.; Singapore; On-site; SGD 42,000 - 54,000; Full time

Job summary

Orion Group Life Sciences is recruiting a Biotechnologist on behalf of a multinational biopharmaceutical client in Tuas, Singapore, for an initial 12-month contract with potential extension.

The role suits fresh graduates and those with 0–1 years of experience, offering exposure to biopharmaceutical manufacturing, quality testing, and batch documentation in a cGMP environment. Rotational shifts may apply.

Qualifications

• NITEC or Diploma in Science, Engineering or a related discipline.
• Fresh graduates with 0–1 years' experience are welcome to apply.
• Biotech/pharma manufacturing experience is helpful but not required.
• Knowledge of cGMP and regulatory requirements is preferred.
• Familiarity with SAP, LIMS or MES is beneficial.
• Strong problem-solving and troubleshooting skills are expected.
• Able to work independently and in a team.
• Willingness to work rotational shifts is required.

Responsibilities

• Perform manufacturing operations in compliance with cGMP and safety requirements.
• Carry out equipment cleaning, setup and manufacturing activities across production areas: Upstream, Downstream, Central Services.
• Complete daily manufacturing tasks as assigned by the Lead Biotechnologist or Supervisor.
• Maintain accurate batch documentation and production records.
• Review documentation for completeness and accuracy; resolve errors.
• Support inventory management and plant upkeep during shifts.
• Report processing abnormalities and equipment issues to supervisors.
• Assist in preparation for regulatory audits and inspections.
• Follow production schedules and EHS procedures.

Skills

Problem solving

Communication

Teamwork

Rotational shifts

Education

NITEC or Diploma in Science, Engineering or a related discipline

Fresh graduates with 0–1 years' experience welcome

Tools

SAP

LIMS or MES

Job description

Orion Group Life Sciences are currently recruiting a Biotechnologist on behalf of our multinational biopharmaceutical client based in Tuas, on an initial 12-month contract with potential to extend.

This position is suitable for junior candidates and fresh graduates looking to gain experience in biopharmaceutical manufacturing.

Position Summary

The Biotechnologist will support cGMP manufacturing operations within a biologics production facility, including equipment setup, manufacturing activities, quality testing and batch documentation.

The role involves supporting daily production operations, troubleshooting activities and ensuring manufacturing processes are carried out in accordance with quality, safety and production requirements.

Key Responsibilities

• Perform manufacturing operations in compliance with cGMP and safety requirements.

• Carry out equipment cleaning, setup and manufacturing activities across relevant production areas, including:

  • Upstream: Vial thaw, inoculation, cell culture and recovery.

  • Downstream: Chromatography, filtration, ultrafiltration and final filling.

  • Central Services: Buffer and media preparation, autoclaving, glass washing, cleaning processes and raw material sampling.

• Complete daily manufacturing tasks as assigned by the Lead Biotechnologist or Manufacturing Supervisor.

• Maintain accurate and timely batch documentation and production records.

• Review documentation for completeness and accuracy, resolving errors where required.

• Support inventory management and general plant upkeep during shifts.

• Report processing abnormalities, equipment issues and unplanned downtime to the relevant supervisor.

• Support preparation for regulatory audits and inspections.

• Follow production schedules, training requirements and EHS procedures.

Qualifications & Experience

• NITEC or Diploma in Science, Engineering or a related discipline, or equivalent qualification.

• Fresh graduates and candidates with 0–1 years' experience are welcome to apply.

• Previous experience in biotechnology, pharmaceutical manufacturing or a related industry would be advantageous but is not essential.

• Knowledge of cGMP and manufacturing regulatory requirements is preferred.

• Familiarity with SAP, LIMS or MES systems would be beneficial.

• Good problem-solving and troubleshooting skills.

• Ability to work independently and communicate effectively within a team.

• Willingness to work rotational shifts is required.