Manufacturing Biotechnologist Upstream (Pharma/Biopharma) New 🔥
Responsibilities:Â
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 software / 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
Must be able to do rotating 12-hour shift work (day and night shifts)
Requirements:
Bachelor Degree 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.
Must be able to carry heavy load (boxes) of up to 15kgs (where applicable).
Must be able to transport boxes within work location with the aid of trolleys.
Must be able to perform work on foot for approximately 2 to 3 hours daily.
Must be able to don varying degrees of gowning throughout the day, depending on the location of the assigned task.
Team player that possesses troubleshooting and analytical skills