Job Description

• To design bio/pharmaceutical manufacturing process and facility (concept, basic and detailed design) in close cooperation with other disciplines.
• Responsible to compile related design documents e.g., process flow diagrams, user requirement specifications (URS), tender specifications (TS), P&IDs, etc.
• Responsible for engineering execution and project management during plant construction, commissioning, and qualification.
• Technical and commercial review of quotations/bids.
• Attend meetings with users/customers/external parties.
• Commission and qualify process and equipment according to cGMP and other relevant regulations.
• Liaise with local authorities during the application and approval process.
• Coordination with other disciplines, partners, sub-consultants, sub-contractors, etc.
• To support the business development efforts in the feasibility study and proposal stage and assist in the technical presentation to clients.

Job Requirements

• Fresh graduates/juniors are encouraged to apply.
• Candidate must possess at least a bachelor’s degree in Pharmaceutical Engineering, Chemical, Biotechnology, Science, or equivalent.
• Working experiences in the pharmaceutical or biotech industries will be an added advantage.
• Preferable with knowledge of cGMP compliance and associated legislative standards, i.e., PIC/s, EU GMP, and US FDA standards for the pharmaceutical industry.
• Familiar with preparation and execution of commissioning and qualification protocols.
• Proficient with AutoCAD, MS Project, and MS Office applications.
• Willingness to learn and pick up new skills and knowledge with open hearts.
• Ability to communicate in Chinese is a plus.

Skills