Biotechnologist | cGMP Manufacturing & Bioprocess Operations #HDC1

RECRUIT EXPRESS PTE LTD; Singapore; Hybrid; SGD 45,000 - 65,000; Full time

Job summary

RECRUIT EXPRESS PTE LTD invites applications from biotech professionals to join a hands-on manufacturing team in a regulated environment. You will engage in day-to-day production, gain exposure to cleanroom operations, MES, validation, troubleshooting, and continuous improvement while collaborating with cross-functional teams to ensure compliant, reliable output.

The role emphasizes hands-on experience in bioprocessing, quality systems, and manufacturing equipment within a GMP framework,

Qualifications

• Strong analytical and problem-solving abilities
• Experience in regulated manufacturing environments is advantageous
• Knowledge of cGMP and cleanroom practices is preferred

Responsibilities

• Perform routine and non-routine manufacturing activities per SOPs and batch records
• Carry out cleanroom production activities including equipment preparation and material handling
• Operate and monitor manufacturing equipment and MES in accordance with GMP requirements
• Conduct production sampling and process monitoring with accurate data recording
• Support deviation investigations and CAPA to maintain manufacturing performance
• Participate in process transfers, equipment qualification, validation and continuous improvement
• Maintain accurate production records and ensure audit readiness

Skills

Analytical skills

Problem solving

Education

Biotechnology

Biomedical Sciences

Chemical Engineering

Applied Chemistry

Pharmaceutical Technology

Tools

MES

Job description

Apply Your Biotechnology Expertise in a Hands-On Manufacturing Environment

Looking to build practical experience inbiotechnology manufacturing, cGMP operations, and bioprocessing?

Join a regulated manufacturing environment where you’ll play an active role in day-to-day production while gaining exposure to cleanroom operations, manufacturing equipment, process systems, validation, troubleshooting, and continuous improvement.

Working alongside Manufacturing, Quality, Engineering, and Technical teams, you’ll contribute to safe, compliant, and reliable production while developing valuable hands-on experience within a structured GMP environment.

What You’ll Be Doing

• Perform routine and non-routine manufacturing activities in accordance with approved SOPs, batch records, and electronic documentation requirements.

• Carry out cleanroom production activities, including equipment preparation, cleaning, sterilisation, filtration, and material handling.

• Operate and monitor manufacturing equipment, process control systems, andManufacturing Execution Systems (MES)in accordance with GMP requirements.

• Conduct production sampling, process monitoring, and relevant laboratory checks while ensuring manufacturing data is accurately recorded.

• Support troubleshooting, deviation investigations, andCorrective and Preventive Actions (CAPA)to maintain consistent manufacturing performance.

• Participate in process transfers, equipment commissioning, qualification, validation, and continuous improvement initiatives.

• Maintain accurate production records, logbooks, and electronic documentation in line with quality and regulatory requirements.

• Support workplace safety, housekeeping, audit readiness, and quality initiatives within the manufacturing facility.

• Share technical knowledge and provide on-the-job guidance to colleagues when required.

• Collaborate with Quality, Engineering, Technical, Manufacturing, and other cross-functional teams to support efficient and reliable operations.

What We’re Looking For

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

• Experience in biotechnology, pharmaceutical, biopharmaceutical, or other regulated manufacturing environments will be advantageous.

• Knowledge ofcGMP requirements, cleanroom practices, manufacturing systems, and production equipmentis preferred.

• Strong analytical and problem-solving abilities with good attention to detail.

• Comfortable working in a fast-paced production environment and supporting rotating shifts where required.

• Able to follow cleanroom gowning procedures, workplace safety requirements, and established manufacturing practices.

• Dependable, detail-oriented, and committed to maintaining high standards of quality, compliance, and operational excellence.

Why Consider This Opportunity?

Gain valuable hands-on exposure acrosscGMP manufacturing, cleanroom operations, bioprocess equipment, validation, process transfers, troubleshooting, and continuous improvement.

This role provides an opportunity to apply your scientific knowledge in a real manufacturing setting while contributing to the production of high-quality biopharmaceutical products and developing practical technical expertise.

If you’re ready to take your biotechnology knowledge into a dynamic manufacturing environment, we welcome your application.