M&s-ifb-quality Manager-mes

Sanofi

Beijing, China
Mes implementation experience in pharmaceutical industry
Knowledge of gmp and fda/eu/china regulations
Experience with smart factory initiatives
The Quality Manager MES-IFB is responsible for ensuring all Quality Assurance activities for the new state-of-the-art insulin facility in Beijing are executed on time and in compliance with global and local regulations

Job Summary

  • The Quality Manager MES-IFB is responsible for ensuring all Quality Assurance activities for the new state-of-the-art insulin facility in Beijing are executed on time and in compliance with global and local regulations.
  • This role serves as the primary Subject Matter Expert for Quality Assurance, overseeing validation strategies, electronic batch record development, and continuous improvement within a fully automated biologics environment.
  • Sanofi offers a supportive future-focused team with extensive growth opportunities, a comprehensive rewards package, and high-quality healthcare benefits including gender-neutral parental leave.

Matching Summary

The Quality Manager MES-IFB is responsible for ensuring all Quality Assurance activities for the new state-of-the-art insulin facility in Beijing are executed on time and in compliance with global and local regulations.

Skills & Requirements

Must-have

  • MES implementation experience in pharmaceutical industry
  • Knowledge of GMP and FDA/EU/China regulations
  • Experience with Smart factory initiatives
  • Proficiency in electronic batch record design
  • Fluent Chinese and English communication skills

Nice-to-have

  • Experience with LIMS and SAP systems
  • Background in API manufacturing processes
  • Strong cross-functional collaboration skills
  • Innovative thinking and change driving ability
  • Leadership and assertiveness in decision-making

Key Requirements

  • 3-5 years industry experience in biopharma or regulated industry
  • MSc level qualification in Science, Pharmacy, or Computer Science
  • Fluent written and spoken Chinese and English
  • Practical experience in MES implementation within pharma
  • In-depth knowledge of API manufacturing process requirements

Work Rights

Not specified

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