The role involves providing Quality oversight and advice to ensure Tuas Singapore GMP Quality operations meet Sanofi global standards
Job Summary
The role involves providing Quality oversight and advice to ensure Tuas Singapore GMP Quality operations meet Sanofi global standards.
Incumbents will participate in Engineering, Commissioning, and Qualification activities including reviewing documents and supporting digital infrastructure setup.
The position requires working 12-hour rotating shifts during PPQ runs and routine operations to support production activities.
Matching Summary
The role involves providing Quality oversight and advice to ensure Tuas Singapore GMP Quality operations meet Sanofi global standards.
Skills & Requirements
Must-have
GMP operations oversight experience
Deviation and CAPA management expertise
Engineering commissioning support
PPQ run quality support
Digital manufacturing systems knowledge
Nice-to-have
Vaccine or biologics industry background
Facility start-up experience
Agile methodology mindset
Regulatory inspection interaction skills
SAP system familiarity for batch release
Key Requirements
Bachelor's or Master's Degree in Sciences or Engineering
Minimum 4 years of relevant pharmaceutical industry experience
Expert knowledge of cGMP regulations and Data Integrity Requirements