Biotechnologist II

Overview: Our client, aleading biopharmaceutical manufacturer, is seeking a Biotechnologist II to support cGMP biologics manufacturing operations within a production facility in Singapore. The successful candidate will be responsible for executing upstream, downstream, and support manufacturing activities while ensuring compliance with quality, safety, and regulatory requirements. The role operates in a team-based manufacturing environment and requires rotational shift work.

Location: Singapore

Key Responsibilities:

Manufacturing Operations

• Execute manufacturing operations in accordance with cGMP, site procedures, and safety requirements.
• Perform equipment cleaning, preparation, setup, and operational activities.
• Support biologics manufacturing processes including:
• Upstream processing (Vial Thaw, Inoculation, Cell Culture and Recovery)
• Downstream processing (Chromatography, Filtration, Ultrafiltration, Final Filling)
• Central Services activities (Buffer/Media Preparation, Autoclave, Glasswash Operations,Cleaning Activities, and Raw Material Sampling)
• Perform daily tasks assigned by the Lead Biotechnologist or Manufacturing Supervisor.

Documentation & Compliance

• Complete batch records and manufacturing documentation accurately, legibly, and in a timely manner.
• Review documentation to ensure completeness and accuracy.
• Support timely resolution of documentation discrepancies and batch record errors.
• Maintain compliance with regulatory, quality, and cGMP requirements.

Production Support & Troubleshooting

• Support production schedules and manufacturing plans.
• Assist in troubleshooting manufacturing issues during shift operations.
• Escalate process deviations, equipment issues, and unplanned downtime to supervisors promptly.
• Maintain appropriate inventory levels to support continuous operations.
• Ensure all required training is completed and remains current.

Safety & Quality

• Adhere to all Environmental, Health and Safety (EHS) policies and standards.
• Support audit and inspection readiness activities.
• Contribute to maintaining overall plant housekeeping and operational readiness during assigned shifts.

Requirements:

Education

• NITEC, Diploma, or equivalent qualification in Biotechnology, Life Sciences, Engineering, Chemical Engineering, or a related discipline.

Experience

• Minimum 2 years of relevant experience in biotechnology, pharmaceutical, biologics, or GMP manufacturing environments.
• Experience in biologics manufacturing operations is advantageous.
• Experience working in regulated manufacturing environments is preferred.

Technical Knowledge

• Understanding of cGMP manufacturing requirements and quality systems.
• Familiarity with manufacturing systems such as SAP, LIMS, and MES is advantageous.
• Knowledge of upstream or downstream biologics manufacturing processes is beneficial.

Soft Skills

• Strong attention to detail and documentation accuracy.
• Good problem-solving and troubleshooting skills.
• Able to work independently and collaboratively within a team environment.
• Good communication and interpersonal skills.

Preferred Skills:

• Biologics manufacturing experience
• GMP documentation and batch record management
• Process troubleshooting
• SAP, LIMS and MES systems
• Continuous improvement mindset
• Shift operations experience

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

EA Reference: R25150511, Cammy Li Xin Hui

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