Manufacturing Biotechnologist Upstream (Pharma/Biopharma)

NUSANTARA PRIME CONSULTING PTE. LTD.; Singapore; On-site; SGD 3,200 - 5,400; Part time

Job summary

NUSANTARA PRIME CONSULTING PTE. LTD. is seeking a biotechnologist to perform routine manufacturing processes, monitor GMP-compliant operations, and support production activities in Singapore.

The ideal candidate has a degree in chemical engineering, pharmaceutical, or biotech, at least 1 year of relevant experience, and is able to work rotating 12-hour shifts. Fresh graduates welcome.

Qualifications

• Degree/Diploma/ITE in chemical engineering, pharmaceutical or biotechnology equivalent.
• Minimum 1-year relevant biotechnologist experience, GMP and/or upstream experience preferred; fresh graduates welcome.
• Basic knowledge in Fermentation, Cell culture, media and buffer preparation, and downstream processing is a plus.
• Willingness to work rotating 12-hour shifts.
• Team player with troubleshooting and analytical skills.

Responsibilities

• Perform routine manufacturing processes and equipment preparation (CIP, PT, SIP).
• Support production activities and record data per EBR in GMP/ EH&S guidance.
• Monitor equipment and process performance.
• Communicate safety, quality, and process issues to supervisor.
• Troubleshoot process-related problems.
• Maintain 5S/Kanban in the production area.
• Review activity documentation per GDP.
• Use LIMS, SAP, DCS, MES to collect and evaluate data.
• Maintain training records and requirements.
• Handle other duties as assigned.

Skills

Troubleshooting

Analytical skills

Team player

Communication

Education

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

Tools

LIMS

SAP

DCS

MES

Job description

Responsibilities

• Perform routine manufacturing processes and equipment preparation (CIP, PT, SIP, etc.)
• Support day to day production activities and record data according to Electronic Batch Record (EBR) in compliance with GMP, Environmental, Health and Safety guidelines.
• Perform equipment and process monitoring
• Able to communicate with Supervisor/supporting functions for any safety, quality, and process irregularities
• Troubleshoot and resolve process related issues.
• Able to perform production area housekeeping (5S, Kanban, etc.)
• Review documentation of activities as per GDP (Good Documentation Practice)
• Use sophisticated softwares / programs (LIMS, SAP, DCS, MES, etc.) to collect and evaluate data
• Responsible for maintaining and meeting training requirements.
• Any other task as assigned by Supervisor/Manager

Requirements

• Degree/Diploma/ITE in chemical engineering, pharmaceutical or biotechnology equivalent
• Minimum 1-year relevant biotechnologist experience, experienced in GMP and/or Upstream. Fresh graduates are welcome to apply.
• Basic skills and knowledge in Fermentation Cell culture, Bioreactor processing, Media and Buffer Preparation and downstream processing is an added advantage.
• Able to do rotating 12-hour shift work
• Team player that possesses troubleshooting and analytical skills
• Must be able to carry heavy load of up to 10kgs
• 1 year contract. Option to extend/annual renewal depending on performance