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
About You:
Degree/Diploma in chemical engineering, pharmaceutical or biotechnology equivalent
1 to 5 years relevant biotechnologist experience, experienced in GMP Upstream, Downstream
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 shift work
Team player that possesses troubleshooting and analytical skills
Must be able to carry heavy load of up to 10kgs
Only shortlisted candidates will be notified.
Contract length: 12 Months. Option to extend depending on performance and business needs.
Location: Tuas
Job Types: Contract, Permanent
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