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

We regret that only shortlisted candidates will be notified.
GMP Technologies (S) Pte Ltd | EA Licence: 11C3793 | EA Personnel: Fiona Koh | Registration No: R1109239