Biotechnologist | cGMP Manufacturing & Process Operations Specialist #HDCE

RECRUIT EXPRESS PTE LTD; Singapore; On-site; SGD 60,000 - 90,000; Full time

Job summary

RECRUIT EXPRESS PTE LTD is seeking a manufacturing professional to support end-to-end cGMP production in a regulated biotechnology environment. The role focuses on ensuring smooth manufacturing processes, process improvement, and operational excellence.

Responsibilities include executing manufacturing activities per SOPs, performing cleanroom tasks, operating equipment, and maintaining accurate documentation to support compliance and safety in a fast-paced setting.

Qualifications

• Degree in Biotechnology, Biomedical Sciences, Chemical Engineering, Applied Chemistry, Pharmaceutical Technology, or related discipline.
• Experience in regulated manufacturing environments (biotech/pharma) is advantageous.
• Knowledge of cGMP and cleanroom practices is preferred.

Responsibilities

• Execute routine and non-routine manufacturing activities per SOPs and batch records.
• Perform cleanroom operations including equipment setup, cleaning, sterilisation, filtration, and material handling.
• Operate and monitor manufacturing equipment and process control systems while maintaining GMP compliance.
• Conduct production sampling, process checks, and accurate recording of manufacturing data.
• Assist with troubleshooting, deviation investigations, and corrective actions to maintain efficiency.
• Support process transfer, validation, equipment commissioning, and continuous improvement initiatives.
• Maintain accurate batch records, logbooks, and production documentation.
• Contribute to workplace safety, quality standards, and audit readiness.

Skills

Attention to detail

Teamwork

Problem solving

Education

Biotech/Pharma degree

Job description

Step into a key role within a regulated biotechnology manufacturing environment!

Join a high-quality production team where you will support end-to-end cGMP manufacturing operations, ensure smooth production processes, and contribute to process improvement and operational excellence.

Key Responsibilities:

• Execute routine and non-routine manufacturing activities in accordance with SOPs, batch records, and electronic documentation systems.
• Perform cleanroom operations including equipment setup, cleaning, sterilisation, filtration, and material handling.
• Operate and monitor manufacturing equipment, process control systems, and electronic manufacturing systems while maintaining GMP compliance.
• Conduct production sampling, process checks, monitoring activities, and accurate recording of manufacturing data.
• Assist with troubleshooting, deviation investigations, corrective actions, and other activities to maintain efficient production operations.
• Support process transfer, validation, equipment commissioning, and continuous improvement initiatives.
• Maintain accurate batch records, logbooks, and production documentation in line with regulatory and quality requirements.
• Contribute to workplace safety, quality standards, housekeeping, and audit readiness within the manufacturing facility.
• Share technical knowledge and provide operational support to team members where required.

Requirements:

• Degree in Biotechnology, Biomedical Sciences, Chemical Engineering, Applied Chemistry, Pharmaceutical Technology, or a related discipline.
• Experience within biotechnology, pharmaceutical, biomedical, or other regulated manufacturing environments will be advantageous.
• Knowledge of cGMP, cleanroom practices, manufacturing systems, and production equipment is preferred.
• Strong attention to detail with good problem-solving and teamwork skills.
• Comfortable working in a fast-paced manufacturing environment with rotating shifts and operational requirements.
• Able to adhere to cleanroom gowning procedures, safety standards, and manufacturing protocols.