Knowledge of China and oversea GMP (NMPA, ISPE, ASME BPE, EP, USP)
• HAZOP Studies when required.
• Familiar with pharmaceutical system validation guidelines.
• Sound knowledge of system design, applicable codes and cGMP’s as they affect process design and equipment specification and knowledge of pharmaceutical production
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• Possesses a demonstrated ability for analytical thinking, an aptitude for structured problem solving, superior verbal and written communication skills as well as a strong work ethic.
• Must be able to build strong rapport within department and across Exyte disciplines.
• Travel may be required as projects are being executed at different parts of China.
• Knowledge of equipment design and system specifications, utility system calculations and energy optimizations
• Knowledge of installation, start-up and commissioning; handover of documentation activities
• Diligence to solve problems and finish the work in a structured manner
• Global mindset and enjoy working in a multi-cultural environment
• Result-oriented and have a well-structured approach to your work
• You have a personal drive and are passionate about your work
Professional experience & education:
• Minimum of fifteen (15)years in bio process design,preferably in the pharmaceutical and biotechnology industries.
• Experience in the life sciences (pharmaceutical,biotech, nutraceutical, etc.)is preferred.
• Bachelor of Science or Bachelor of Engineering (Hons) Degree (orequivalent) in Engineering。