Manufacturing Biotechnologist

TEKsystems; Singapore; On-site; SGD 50,000 - 73,000; Full time

Job summary

Allegis Group Singapore Pte Ltd is seeking a Biomanufacturing Operator to execute upstream, downstream, and central services in a cGMP environment. The role involves operating bioprocess equipment and ensuring manufacturing activities align with approved batch records and SOPs.

The candidate should have 1–4 years of experience in biopharmaceutical or manufacturing settings, with strong documentation and cleanroom discipline.

Qualifications

• GMP understanding and compliant documentation habits.
• Experience with bioprocess equipment is advantageous.
• Comfortable in cleanroom environments and strict procedures.

Responsibilities

• Execute upstream, downstream and central biomanufacturing processes per batch records and SOPs.
• Operate bioprocess equipment (bioreactors, centrifuges, chromatography, buffers) and related manufacturing equipment.
• Ensure production activities comply with cGMP requirements and production schedules.
• Maintain GMP documentation and participate in investigations or deviations as needed.
• Support technology transfer, process validation and continuous improvement.

Skills

GMP knowledge

Documentation & communication

Cleanroom practices

Education

Diploma or Degree in Biotechnology/Life Sciences/Bioprocess Tech/related

Tools

Bioreactors

Centrifuges

Chromatography systems

Buffer preparation systems

Job description

• Execute upstream, downstream and/or central services biomanufacturing processes in accordance with approved batch records and SOPs
• Operate bioprocess equipment such as bioreactors, centrifuges, buffer preparation systems, chromatography systems and related manu
• Ensure production activities are completed according to cGMP requirements and production schedules.

• Execute upstream, downstream and/or central services biomanufacturing processes in accordance with approved batch records and SOPs
• Operate bioprocess equipment such as bioreactors, centrifuges, buffer preparation systems, chromatography systems and related manu
• Ensure production activities are completed according to cGMP requirements and production schedules.

Key Responsibilities

• Execute upstream, downstream and/or central services biomanufacturing processes in accordance with approved batch records and SOPs.
• Operate bioprocess equipment such as bioreactors, centrifuges, buffer preparation systems, chromatography systems and related manufacturing equipment.
• Ensure production activities are completed according to cGMP requirements and production schedules.

Manufacturing Operations

• Execute upstream, downstream and/or central services biomanufacturing processes in accordance with approved batch records and SOPs.
• Operate bioprocess equipment such as bioreactors, centrifuges, buffer preparation systems, chromatography systems and related manufacturing equipment.
• Ensure production activities are completed according to cGMP requirements and production schedules.

Quality & Compliance

• Perform in-process sampling, testing and monitoring of critical quality attributes.
• Maintain accurate and complete GMP documentation, including electronic batch records.
• Adhere to cleanroom requirements, biosafety procedures and EHS regulations.

Equipment & Process Support

• Conduct equipment cleaning, sanitisation and preparation activities.
• Participate in investigations related to manufacturing deviations and support corrective actions.
• Support technology transfer, process validation and continuous improvement initiatives.

Requirements

• Diploma or Degree in Biotechnology, Life Sciences, Biological Sciences, Bioprocess Technology, Chemical Engineering or a related discipline.
• 1 to 4 years of experience in biopharmaceutical, biotechnology, pharmaceutical or manufacturing environments.
• Understanding of GMP and regulated manufacturing environments.
• Experience operating bioprocess equipment is advantageous.
• Comfortable working in a cleanroom environment and following strict compliance procedures.
• Good documentation and communication skills.

Preferred Skills

• Upstream or downstream bioprocessing experience.
• Knowledge of bioreactors, chromatography, filtration or centrifugation systems.
• Experience with electronic batch records (EBR).
• Familiarity with process validation and technology transfer activities.
• Strong attention to detail and problem-solving skills.

We regret to inform that only shortlisted candidates will be notified.

Job Reference: R25150511 Cammy Li Xin Hui

Allegis Group Singapore Pte Ltd, Company Reg No. 200909448N, EA License No. 10C4544