Contract Biotechnologist – GMP Required – Pharma MNC (1 Year, Shift Work) #HVY

RECRUIT EXPRESS PTE LTD

Singapore

On-site

SGD 40,000 - 64,000

Full time

4 days ago
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Job summary

RECRUIT EXPRESS PTE LTD is seeking a Cell Culture and Purification Technician to perform manufacturing operations under cGMP. You will follow SOPs, record data, monitor equipment, and apply aseptic technique across shifts.

The role requires GMP experience, strong documentation, and the ability to troubleshoot process issues while maintaining accurate records. Overtime and shift work are expected in a fast-paced biotech environment.

Qualifications

  • Must have GMP experience and strong documentation practices.
  • Ability to troubleshoot process issues and record data accurately.
  • Willing to work shifts, holidays, and overtime.

Responsibilities

  • Perform routine and critical manufacturing operations in Cell Culture and Purification under cGMP
  • Follow SOPs and record data in EBM/MBRs/MFRs
  • Monitor equipment
  • Perform basic lab tests (sampling, pH, conductivity)
  • Apply aseptic technique
  • Troubleshoot process issues
  • Maintain accurate documentation
  • Support equipment cleaning, assembly/disassembly, 5S, and changeover activities

Skills

GMP experience
Documentation
Communication
Troubleshooting
Computer skills

Education

Bachelors or higher in Chemical/Bioengineering/Pharmaceutical Engineering
Diploma in related science/engineering biotech/pharma

Job description

About the role

Perform routine and critical manufacturing operations in Cell Culture and Purification under cGMP. Follow SOPs, record data in EBM/MBRs/MFRs, monitor equipment, perform basic lab tests (sampling, pH, conductivity), apply aseptic technique, troubleshoot process issues, and maintain accurate documentation. Support equipment cleaning, assembly/disassembly, 5S, and changeover activities.

Key responsibilities
  • Perform routine and critical manufacturing operations in Cell Culture and Purification under cGMP
  • Follow SOPs and record data in EBM/MBRs/MFRs
  • Monitor equipment
  • Perform basic lab tests (sampling, pH, conductivity)
  • Apply aseptic technique
  • Troubleshoot process issues
  • Maintain accurate documentation
  • Support equipment cleaning, assembly/disassembly, 5S, and changeover activities
About you
  • Degree in Chemical/Bioengineering/Pharmaceutical Engineering or Diploma in related science/engineering biotech/pharma
  • GMP experience required
  • Good documentation, communication, troubleshooting, and computer skills
  • Willing to work shifts, holidays, overtime
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