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 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