Responsibilities

• Assist the Production Manager to plan and organize the production department to achieve company’s business objectives
• Ensure compliance to the regulatory requirements of all products manufactured
• Monitor the equipment, cleanroom and warehouse according to the approved PIC/S GMP procedures
• Involve in design of various manufacturing process flows and monitoring of Process Validation & Cleaning Validation processes;
• Manage GMP documents e.g. batch production records, manufacturing instructions, SOPs, etc.
• Work closely with QA, QC and R&D departments to achieve company’s goals on productivity and quality
• Stem cell product manufacturing and packaging
• Other duties as assigned by Production Manager and/or management team.
  
  
  

Requirements

• Bachelor or above biotechnology, biochemistry, chemistry and medical laboratory science or science degree with relevant to cell therapy, gene therapy, regenerative medicines or tissue engineering, or other similar sciences disciplines;
• At least 4 years’ significant experience of production/manufacturing role in a PIC/S GMP compliant organisation
• Good organization, communication, management and training skills.
• Independent, enthusiastic and a good team player
• Proficiency in English and Chinese.
  
  
  

We offer an attractive remuneration package including group medical insurance, discretionary year-end performance bonus, and an energetic, fun work environment.

Interested parties please send your resume with current, expected salary and availability to the HR Department.

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