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
Minimum 1 year relevant biotechnologist experience, experienced in GMP Upstream, Downstream, fresh Diploma graduate is 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 shift work
Team player that possesses troubleshooting and analytical skills
Must be able to carry heavy load of up to 10kgs
Contract length: 12 Months. Option to extend depending on performance and business needs.Job Type: Contract Location: TuasAll staff to observe MOH regulations and practicesJob Types: Full-time, Contract Contract length: 12 monthsSalary: $2,000.00 - $3,500.00 per monthSchedule:
Monday to Friday
Supplemental Pay:
Overtime pay
Experience:
Pharma Industry: 1 year (Preferred)
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