
Manufacturing Biotechnologist Upstream
4 days ago
**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
**About You**:
- Degree/Diploma/ITE in chemical engineering, pharmaceutical or biotechnology equivalent
- Minimum 1 year relevant biotechnologist experience, experienced in GMP and/or Upstream. **Fresh graduate is 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
**Job Types**: Contract, Permanent
Contract length: 12 months
**Salary**: $2,000.00 - $2,800.00 per month
**Benefits**:
- Promotion to permanent employee
Schedule:
- Monday to Friday
Supplemental pay types:
- Overtime pay
COVID-19 considerations:
All staff to observe MOH regulations and practices.
**Experience**:
- Pharma/Biopharma: 1 year (preferred)
- GMP and/or Upstream process: 1 year (preferred)
Shift availability:
- Day Shift (preferred)
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