GMP Upstream Bioprocess Scientist

No-Deviation-Pte.-Ltd; Singapore; On-site; SGD 60,000 - 90,000; Full time

Benefits offered by this job

Generous Leave Policy

Health & Wellness Coverage

Professional Development

Inclusive Culture

Impactful Projects

Job summary

No deviation is seeking an Upstream Biotechnologist to support GMP biologics manufacturing. You will engage in upstream cell culture, equipment preparation, process monitoring, sampling, troubleshooting, and comprehensive GMP documentation.

The role emphasizes cross-functional collaboration with Manufacturing, MSAT, QC, QA and Engineering to ensure compliant production and continuous improvement in a dynamic biotech environment.

Qualifications

• GMP knowledge and adherence to documentation practices are essential.
• Proven ability to document processes, deviations, and CAPA actions.
• Hands-on experience with upstream cell culture and bioreactor operations is preferred.
• Familiarity with batch records and data integrity principles is important.
• Willingness to support shift work and manufacturing schedules.

Responsibilities

• Perform and support upstream manufacturing activities, including cell thawing, seed train expansion, inoculation and cell culture.
• Monitor critical process parameters such as pH, temperature, DO, agitation and gas flow.
• Operate bioreactors and assist in single-use or stainless-steel systems setup.
• Support CIP/SIP cleaning and sterilisation activities where applicable.
• Maintain GMP documentation and batch records in compliance with ALCOA+ principles.
• Assist in investigations of deviations and CAPA, and support technology transfer and process validation.

Skills

GMP knowledge

Documentation skills

Troubleshooting

Cross-functional teamwork

Shift flexibility

Education

Bachelor's or Diploma in Biotechnology / Biochemistry / Chemical Engineering / Life Sciences

Tools

Single-use systems

CIP/SIP

Job description

No deviation is seeking an Upstream Biotechnologist to support GMP biologics manufacturing. You will engage in upstream cell culture, equipment preparation, process monitoring, sampling, troubleshooting, and comprehensive GMP documentation.

The role emphasizes cross-functional collaboration with Manufacturing, MSAT, QC, QA and Engineering to ensure compliant production and continuous improvement in a dynamic biotech environment.