Regulatory Affairs Specialist
il y a 4 semaines
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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