Regulatory Affairs Specialist

il y a 4 semaines


Courbevoie, Île-de-France ProductLife Group Temps plein

Regulatory Affairs Specialist

We are seeking a highly skilled Regulatory Affairs Specialist to join our team at ProductLife Group. As a key member of our team, you will be responsible for coordinating and managing the Linguistic Review process for Centralized Procedure medicinal products.

About the Role

The successful candidate will have a strong background in regulatory labelling procedures and experience in project coordination/management. You will be responsible for managing the relationship with our translation partner and ensuring the smooth coordination of Linguistic Review processes with internal and external stakeholders.

Key Responsibilities

  • Coordinate and manage the Linguistic Review process for Centralized Procedure medicinal products
  • Manage the relationship with our translation partner
  • Ensure the smooth coordination of Linguistic Review processes with internal and external stakeholders
  • Provide ongoing support to project teams

Requirements

  • At least a Bachelor's Degree in Life Sciences
  • At least 1-2 years' experience in Regulatory Labelling Operations in a Pharmaceutical Company or Service Provider
  • Good knowledge of regulatory labelling procedures
  • Experience in Project Coordination/Management

What We Offer

We offer a dynamic and challenging work environment, with opportunities for professional growth and development. If you are a motivated and experienced Regulatory Affairs Specialist looking for a new challenge, please submit your application.


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