Mes implementation experience in pharmaceutical industry
Knowledge of gmp and regulatory compliance fda eu china
Experience with smart factory initiatives and digital systems
The Quality Manager MES-IFB is responsible for ensuring all Quality Assurance activities for the new Insulin Drug Substance facility are executed on time and in compliance with regulations
Job Summary
The Quality Manager MES-IFB is responsible for ensuring all Quality Assurance activities for the new Insulin Drug Substance facility are executed on time and in compliance with regulations.
This role involves developing electronic batch record designs, supporting validation strategies, and actively engaging in Smart factory initiatives to meet global standards.
Sanofi offers a supportive team environment with growth opportunities, a comprehensive rewards package, and extensive health and wellbeing benefits including parental leave.
Matching Summary
The Quality Manager MES-IFB is responsible for ensuring all Quality Assurance activities for the new Insulin Drug Substance facility are executed on time and in compliance with regulations.
Skills & Requirements
Must-have
MES implementation experience in pharmaceutical industry
Knowledge of GMP and regulatory compliance FDA EU China
Experience with Smart factory initiatives and digital systems
Nice-to-have
Strong cross-functional collaboration skills
Innovative thinking and change driving capabilities
Fluency in Chinese and English languages
Key Requirements
3-5 years industry experience in biopharma or regulated industry
Degree in Science, Pharmacy, or Computer Science (MSc preferred)
Fluent in both written and spoken Chinese and English