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 help us process your application, please visit www.gmprecruit.com to upload your resume on our website.
GMP Technologies (S) Pte Ltd   |   EA Licence: 11C3793   |  Fiona Koh  |   Registration No: R1109239