About this role
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
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