Ancillary Document Coordinator (french Speaker)

Sanofi Genzyme

Budapest, Hungary
Base: ft9,120,000.00 - ft13,680,000.00; bonus/equi...
Hybrid
Strong french and english language skills
Experience in regulatory operations or affairs
Knowledge of health authority requirements
This role involves managing end-to-end ancillary document requests and ensuring compliance with global regulatory standards

Job Summary

  • This role involves managing end-to-end ancillary document requests and ensuring compliance with global regulatory standards.
  • The position requires direct interaction with French Health Authorities to request CPPs and GMP certificates.
  • Employees enjoy a flexible hybrid work policy, access to an award-winning office, and comprehensive health benefits including parental leave.

Matching Summary

This role involves managing end-to-end ancillary document requests and ensuring compliance with global regulatory standards.

Salary

Base: Ft9,120,000.00 - Ft13,680,000.00; Bonus/Equity: Not specified; Benefits: Eligible for company employee benefit programs

Skills & Requirements

Must-have

  • Strong French and English language skills
  • Experience in Regulatory Operations or Affairs
  • Knowledge of Health Authority requirements
  • Project management for ancillary documents
  • Proficiency with Vault RIM systems

Nice-to-have

  • Ability to work across cultures
  • Process improvement mindset
  • Self-starter motivation
  • Vendor management experience
  • Continuous improvement initiatives

Key Requirements

  • Minimum Bachelor's degree in regulatory affairs or sciences
  • Direct pharmaceutical industry experience preferred
  • Fluent verbal and written French (min. B2)

Work Rights

Not specified

Tailored Resume

Cover Letter