Job Responsibility:

• Establish, implement and maintain the production processes in accordance with the Quality Management System and current Good Management Production (cGMP) production requirement.
• Manage production operations and ensure their strict implementation in accordance with the Bio-Pharmaceutical and Pharmaceutical Quality System. Report and investigate any non-conformity of anything related to lab activities.
• Review and approve internal quality testing on the materials upon usage for manufacturing.
• Liaise with suppliers on the purchasing/maintenance of lab reagents and consumables for lab activities.
• Maintain an up-to-date inventory of materials related to activities in cGMP lab.
• Establish and ensure good documentations for lab production and QC (i.e. SOP, BMR, COA etc.).

Job Qualification:

• The minimum qualification of a Degree in the field of Life Science or a related field.
• Experience in cell culture and aseptic technique is an added advantage.