Responsibilities:
- Perform functions associated with cGMP manufacturing operations within the biologics production facility, including working with engineers in set-up and calibration tasks, as well as performing rework and quality testing related to the production of parts, components and final materials.
- Uses sophisticated programs (such as LIMS, SAP, automated control systems, etc.) to collect and evaluate operating data, which can be used to conduct on-line adjustments to products, instruments or equipment. Determines and may assist in developing methods and procedures to control or modify the manufacturing process
- And any other duties as assigned by supervisor
Requirements:
- Min bachelor's degree in biotechnology
- Able to perform 12 hours rotating day and night shifts
Interested applicants, please email your resume to Alvin Lee Peck Keong
Email: [Confidential Information]
CEI Reg No: R1104781
EA Licence No: 99C4599
