Responsibilities:

• Plan, organize and lead the production department to achieve company’s business objectives
• Act as a key person of a PIC/s standard pharmaceutical plant
• Ensure compliance to health, safety and regulatory requirements of all products manufactured
• Work closely with QA, QC and R&D departments to achieve company’s goals on productivity and quality
• Monitor the equipment, cleanroom and warehouse according to the approved GMP procedures
• Involve in design of various manufacturing process flows in the pharmaceutical plant
• Manage GMP documents e.g. batch production records, manufacturing instructions, SOPs, etc.
• Involve in design and monitoring of Process Validation & Cleaning Validation processes
• Oversee production activities, including control of production process and production facilities
• Perform ad hoc tasks as assigned
   

Requirements:

• Bachelor or above in Science or Engineering related disciplines e.g. Pharmaceutical Technology, Chemical Engineering, Chemistry, Biology, Food Science, Biochemistry, Total Quality Management, etc.
• Minimum 3 years’ experience in GMP biopharmaceutical or pharmaceutical manufacturing field in supervisory or managerial level
• Good organization, communication, management and training skills
• Be accountable and able to solve practical problems in manufacturing

Interested parties please send full resume with present and expected salary to Human Resources Department by clicking "APPLY NOW".

(Information provided will be treated in strict confidence and will only be used for recruitment-related purposes.)