Jobscope:
- Participate in the preparation, operation and completion of assigned process stages to ensure the production of bulk drug substances is within establish timing and quality standards.
- Ensure good housekeeping of the facilities to keep them in good operational order in line with cGMP, safety and environmental requirements.
- Identify areas for improvement and participate in continuous improvement projects to enhance operational effectiveness and efficiencies
- Participate in commissioning and qualification activities as required
- Perform timely review of documentation and make necessary corrections.
- Have good quality mindset and integrity to ensure products are manufactured with the highest quality
- Participate in deviation investigation process
- Reporting and documentation - Ensure that batch record, checklist and logbooks are correctly recorded, cGMP complied and maintained. Perform VS review of completed documentation to ensure adherence to GDP
Requirements:
- Possess (NITEC/HIGHER NITEC/DIPLOMA) in the fields of Biotechnology/Chemical Engineering/Life Science
- Minimum 2 years of relevant experience in Biologics/Chemical/Pharmaceutical/ Food or other regulated industry
- Basic knowledge of cGMP
- Familiar with purification/fermentation/conjugation/isolator operations/material and buffer operations is an advantage
- Candidates with no prior experience will be considered
- Able to perform 12 hours shift and in clean room environment
- Comfortable to perform physical work
To apply, please visit www.gmprecruit.com and search for Job Reference: 24320
To learn more about this opportunity, please contact Fiona Koh
We regret that only shortlisted candidates will be notified.
GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | EA Personnel: Fiona Koh| Registration No: R11092398
