Business Quality Representative For Manufacturing Digital Solutions

Sanofi UK

Budapest, Hungary
Base: ft13,171,200.00 - ft19,756,800.00; bonus/equ...
Hybrid (60% office, 40% home)
Gxp compliance for computerized systems
Data integrity principles (alcoa+)
Computer system validation (csv) activities
Sanofi UK is seeking a Business Quality Representative for its Manufacturing & Supply Digital Solutions team in Budapest, Hungary. The role focuses on ensuring compliance with GxP regulations for computerized systems in the pharmaceutical manufacturing environment while promoting a supportive and innovative workplace culture

Job Summary

  • The Manufacturing & Supply (M&S) Quality Digital Solutions team drives the transformation of Quality operations at Sanofi, simplifying, standardizing, and digitalizing processes across Quality Management Systems (QMS), Quality Control, Supply Chain, Manufacturing, and Analytics-related projects.
  • As a Business Quality Representative, you will play a vital role in supporting quality related activities for digital solutions used in Manufacturing & Supply chain processes, assisting in ensuring that computerized systems comply with GxP regulations and maintain compliance & data integrity.
  • Our Budapest Hub has been recognized for workplace excellence, innovation, and our commitment to putting people first, offering a supportive, future-focused team in an international work environment with a thoughtful rewards package.

Matching Summary

Match Score: 85

Sanofi UK is seeking a Business Quality Representative for its Manufacturing & Supply Digital Solutions team in Budapest, Hungary. The role focuses on ensuring compliance with GxP regulations for computerized systems in the pharmaceutical manufacturing environment while promoting a supportive and innovative workplace culture.

Salary

Base: Ft13,171,200.00 - Ft19,756,800.00; Bonus/Equity: Not specified; Benefits: Company employee benefit programs

Skills & Requirements

Must-have

  • GxP compliance for computerized systems
  • Data integrity principles (ALCOA+)
  • Computer system validation (CSV) activities
  • Review GxP controls in URS and user stories

Nice-to-have

  • Support risk evaluation and CAPA implementation
  • Collaborate with cross-functional teams
  • Proactive problem-solving approach

Key Requirements

  • 5+ years in pharmaceutical quality assurance or GxP computerized systems
  • Degree in Life Sciences, Pharmacy, Engineering, Computer Science, or related field
  • Professional English proficiency

Work Rights

Not specified

Tailored Resume

Cover Letter