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: (HIDDEN TEXT) CEI Reg No: R EA Licence No: 99C4599