N
Manufacturing Biotechnologist
Salary undisclosed
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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
- Must be able to do rotating 12-hour shift work (day and night shifts)
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.
- 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
Job Type: Contract
Contract length: 12 months
Pay: $2,800.00 - $3,800.00 per month
Experience:
- CGMP, clean room: 1 year (Preferred)
- cell culturing, purification, filtration: 1 year (Preferred)
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
- Must be able to do rotating 12-hour shift work (day and night shifts)
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.
- 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
Job Type: Contract
Contract length: 12 months
Pay: $2,800.00 - $3,800.00 per month
Experience:
- CGMP, clean room: 1 year (Preferred)
- cell culturing, purification, filtration: 1 year (Preferred)