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
