Senior Regulatory Affairs Consultant IVDR

2 weken geleden


Amsterdam, Nederland Michael Page Voltijd
Position Overview

Regulatory Affairs Specialist IVDR plays a crucial role in ensuring compliance with regulatory standards in the medical and pharmaceutical sectors.

About the Company

Michael Page is a leading recruitment consultancy with extensive expertise in the pharmaceutical industry. Our client is recognized for their innovative contributions to IVDR and research, focusing on the development and commercialization of essential products.

Key Responsibilities
  • Ensure adherence to regulatory requirements for IVDR products.
  • Collaborate with cross-functional teams to support product development and compliance.
  • Prepare and submit regulatory documentation to relevant authorities.
  • Monitor changes in regulations and assess their impact on the organization.
  • Provide guidance on regulatory strategies and best practices.
Qualifications

The ideal candidate will possess a strong background in regulatory affairs, particularly within the IVDR framework, and demonstrate a commitment to maintaining high standards of compliance.



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