Senior Biotechnologist

ALLEGIS GROUP SINGAPORE PRIVATE LIMITED; Singapore; On-site; SGD 50,000 - 80,000; Full time

Job summary

A leading bioscience company in Singapore is seeking a Biotechnologist for a 12-month contract role. You will contribute to cutting-edge biologics production, ensuring quality and compliance in manufacturing processes. The ideal candidate possesses a degree in Biotechnology or Biochemistry and 2–4 years of relevant experience in biologics manufacturing. Join a dynamic team and thrive in a regulated environment.

Qualifications

• 2–4 years of hands-on experience in biologics manufacturing.
• Solid understanding of cGMP regulations and manufacturing documentation.
• Proficiency in automated systems and data collection tools.

Responsibilities

• Execute upstream and downstream manufacturing processes.
• Operate and monitor automated control systems and equipment.
• Conduct quality testing and review batch records.

Skills

Cell culture

Buffer and media preparation

Column chromatography

Tangential flow filtration

Problem-solving

Communication

Education

Bachelor's degree in Biotechnology, Biochemistry, or related discipline

Tools

LIMS

SAP

Job description

Join its biologics manufacturing team in Singapore. This is a 12-month contract role offering the opportunity to contribute to cutting-edge biologics production in a dynamic and regulated environment.

Role Overview

As a Biotechnologist, you will be responsible for executing and supporting cGMP manufacturing operations within a state-of-the-art biologics facility. You will play a key role in ensuring the quality, efficiency, and compliance of production processes, while collaborating with cross-functional teams to meet operational goals.

Key Responsibilities

• Execute upstream and downstream manufacturing processes, including:
  • Cell culture (from vial thaw to production scale)
  • Buffer and media preparation
  • Column chromatography
  • Tangential flow filtration
  • Sampling of in-process and raw materials
• Operate and monitor automated control systems and equipment (e.g., LIMS, SAP)
• Perform equipment setup, calibration, and routine maintenance
• Conduct quality testing and rework activities
• Review batch records and worksheets for accuracy and completeness
• Support investigations and resolve processing anomalies
• Participate in internal and external audits and inspections
• Manage documentation and demand work orders
• Lead shift activities when required and assign tasks within the team

Qualifications

• Bachelor’s degree in Biotechnology, Biochemistry, or a related discipline
• 2–4 years of hands-on experience in biologics manufacturing, with expertise in either upstream or downstream processes
• Solid understanding of cGMP regulations and manufacturing documentation
• Proficiency in automated systems and data collection tools
• Strong problem-solving and communication skills
• Ability to thrive in a fast-paced, team-oriented environment

Preferred Skills

• Experience in troubleshooting and process optimization
• Familiarity with regulatory compliance and audit readiness

We are an equal opportunities employer and welcome applications from all qualified candidates.