Bioprocess Manufacturing Specialist | cGMP Operations & Process Improvement #HDC1

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

Job summary

RECRUIT EXPRESS PTE LTD seeks a Bioprocess Manufacturing Specialist to join our GMP-regulated biopharmaceutical manufacturing team. You will support day-to-day operations, work with manufacturing processes, equipment, and continuous improvement initiatives to ensure product quality.

You will operate MES and cGMP-controlled processes in cleanroom environments, perform sampling and in-process checks, investigate issues, and collaborate with Quality, Engineering and Technical Operations to keep

Qualifications

• Degree in Biotechnology, Biomedical Sciences, Chemical Engineering, Applied Chemistry, or Pharmaceutical Technology.
• Experience in biotechnology/pharma GMP manufacturing environments is advantageous.
• Strong knowledge of cGMP, cleanroom operations, and manufacturing systems.
• Willingness to support rotating shift schedules.
• Commitment to quality, safety and continuous improvement.

Responsibilities

• Execute day-to-day manufacturing operations per SOPs, batch docs, and electronic systems.
• Support cleanroom manufacturing processes including equipment setup, cleaning, sterilisation, and filtration.
• Operate and monitor manufacturing equipment, process control systems, and MES while complying with cGMP.
• Perform production sampling and in-process checks with accurate documentation.
• Investigate manufacturing issues and assist with deviations, CAPA, and troubleshooting.
• Contribute to process transfer activities, equipment qualification, and validation.
• Ensure production records and logs are complete and compliant.
• Maintain a safe, audit-ready manufacturing environment following safety and quality procedures.
• Provide technical support and share manufacturing knowledge with the team.
• Collaborate with Quality, Engineering, Technical Operations and other functions to sustain smooth production.

Skills

cGMP knowledge

Troubleshooting

Analytical thinking

Cleanroom operations

Cross-functional collaboration

Education

Biotechnology, Biomedical Sciences, Chemical Engineering, Applied Chemistry, Pharmaceutical Technology

Tools

MES

Job description

Advance Your Career in Biopharmaceutical Manufacturing

Looking to build hands-on experience in aGMP-regulated biopharmaceutical manufacturing environment? This opportunity is ideal for biotechnology professionals who enjoy working with manufacturing processes, production equipment, and continuous improvement initiatives.

As aBioprocess Manufacturing Specialist, you will support day-to-day manufacturing operations while gaining exposure tocleanroom production, equipment operations, validation, troubleshooting, process transfer, and manufacturing process improvement. You will work closely with technical and cross-functional teams to ensure production activities are carried out safely, efficiently, and in accordance with established quality standards.

What You’ll Do

• Execute day-to-day manufacturing operations, including both routine and non-routine activities, in line with approved SOPs, batch documentation, and electronic systems.

• Support cleanroom manufacturing processes involving equipment setup, cleaning, sterilisation, filtration, material preparation, and handling.

• Operate and monitor manufacturing equipment, process control systems, and Manufacturing Execution Systems (MES) while maintaining compliance with cGMP requirements.

• Perform production sampling, process monitoring, and relevant in-process checks while ensuring manufacturing information is recorded accurately and promptly.

• Investigate manufacturing issues and assist with troubleshooting, deviation assessments, CAPA, and other activities aimed at maintaining reliable production performance.

• Contribute to process transfer activities, equipment commissioning, qualification and validation exercises, and manufacturing improvement projects.

• Ensure production records, equipment logbooks, electronic records, and other required documentation are complete, accurate, and compliant with quality standards.

• Maintain a safe, clean, and audit-ready manufacturing environment by following established safety, housekeeping, and quality procedures.

• Provide technical support and share relevant manufacturing knowledge with team members where required.

• Work collaboratively with Quality, Engineering, Technical Operations, and other supporting functions to maintain smooth and consistent production activities.

What We’re Looking For

• Degree inBiotechnology, Biomedical Sciences, Chemical Engineering, Applied Chemistry, Pharmaceutical Technology, or a related discipline.

• Relevant experience withinbiotechnology, pharmaceutical, biopharmaceutical, or other GMP-regulated manufacturing environmentswill be advantageous.

• Understanding ofcGMP principles, cleanroom operations, manufacturing processes, production equipment, and manufacturing systemsis preferred.

• Strong troubleshooting, analytical, and problem-solving abilities, with the ability to manage priorities in a production-focused environment.

• Willingness to supportrotating shift schedulesand operational requirements.

• Comfortable working in controlled cleanroom environments and adhering to gowning, safety, and manufacturing procedures.

• Meticulous and dependable, with a strong commitment to quality, compliance, safety, and continuous improvement.

Grow Your Expertise in Bioprocess Manufacturing

Take the opportunity to strengthen your technical capabilities acrosscGMP production, bioprocessing technologies, equipment qualification, validation, and process optimisationwhile contributing to the manufacture of quality biopharmaceutical products.

If you are keen to develop your career in a highly regulated manufacturing environment and apply your scientific knowledge in a practical setting, we welcome your application.