Roles & Responsibilities
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 equivalentMinimum 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 workTeam player that possesses troubleshooting and analytical skillsMust be able to carry heavy load of up to 10kgs1 year contract. Option to extend / annual renewal depending on performance
Tell employers what skills you have
Kanban
Housekeeping
Fermentation
Manufacturing Processes
Upstream
Cell Culture
Environmental Health
Biotechnology
LIMS
Chemical Engineering