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Manufacturing Biotechnologist Downstream/Central Services (Pharma/Biopharma)

NUSANTARA PRIME CONSULTING PTE LTD (Nusaprime)

Singapore

On-site

SGD 60,000 - 80,000

Full time

3 days ago
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Job summary

A consulting firm in Singapore is seeking a Manufacturing Biotechnologist for their Downstream/Central Services team in Pharma/Biopharma. The role involves supporting manufacturing processes while ensuring compliance with GMP and safety guidelines. Candidates with a relevant degree or fresh graduates are encouraged to apply. The position requires a willingness to work rotating 12-hour shifts and the ability to lift up to 10 kg. This opportunity offers full-time employment with a contract length of 12 months.

Qualifications

  • At least 1 year of relevant biotechnologist/laboratory experience; fresh graduates are welcome.
  • Willing to do rotating 12-hour shifts.
  • Capable of lifting up to 10 kg.

Responsibilities

  • Perform routine manufacturing processes and equipment preparation.
  • Support daily production activities and record data according to Electronic Batch Record (EBR).
  • Monitor equipment and processes.

Skills

Team player
Troubleshooting skills
Analytical skills
Knowledge in fermentation
Knowledge in cell culture

Education

Degree/Diploma/ITE in chemical engineering, pharmaceutical, or biotechnology

Tools

LIMS
SAP
DCS
MES

Job description

Manufacturing Biotechnologist Downstream/Central Services (Pharma/Biopharma)

We are hiring a Manufacturing Biotechnologist for Downstream/Central Services in Pharma/Biopharma. The role involves supporting manufacturing processes, equipment preparation, and data recording in compliance with GMP and safety guidelines.

Responsibilities
  • Perform routine manufacturing processes and equipment preparation (CIP, PT, SIP, etc.)
  • Support daily production activities and record data according to Electronic Batch Record (EBR)
  • Monitor equipment and processes
  • Communicate safety, quality, and process issues to supervisors
  • Troubleshoot process-related problems
  • Maintain production area housekeeping (5S, Kanban, etc.)
  • Review documentation in accordance with Good Documentation Practice (GDP)
  • Use softwares such as LIMS, SAP, DCS, MES for data collection and analysis
  • Meet training requirements and perform other tasks as assigned
Requirements
  • Degree/Diploma/ITE in chemical engineering, pharmaceutical, or biotechnology
  • At least 1 year of relevant biotechnologist/laboratory experience; fresh graduates are welcome
  • Knowledge in fermentation, cell culture, bioreactor processing, media and buffer preparation, downstream processing is a plus
  • Willing to do rotating 12-hour shifts
  • Team player with troubleshooting and analytical skills
  • Capable of lifting up to 10 kg
  • Based in Tuas
Additional Details
  • Contract length: 12 months
  • Preferred experience in GMP facilities, fermentation, bioreactor processing, media/buffer prep
  • Seniority level: Entry level
  • Employment type: Full-time
  • Job function: Research, Analyst, IT
  • Industry: Business Consulting and Services

This job is active and accepting applications.

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