Senior Device Regulatory Lead for Global Submissions

Il y a 1 jour

Paris, Île-de-France elemed Temps plein 60 000 € - 80 000 € Contrat
A biopharma company in Paris is seeking a Senior Consultant for Device Regulatory Documentation & Compliance. In this role, you will mentor a team, develop regulatory documentation, and ensure compliance for medical devices and combination products. This opportunity is perfect for someone with 5–7 years of experience in the field, a thorough understanding of regulatory standards, and excellent communication skills. The position offers a supportive and collaborative environment in a fast-paced industry.