Job Description

Location:

Etoy

Start date:

ASAP

Extent:

Full time, 80-100%, 6-month assignment

Type of work:

Staffing

About the role

For our client, a major multinational company, we are looking for a Regulatory Affairs Specialist to join their team ! You will manage the regulatory compliance and product lifecycle of medical devices within a global framework. This role involves close collaboration with R&D and Marketing teams across Switzerland, the US, and Japan to ensure market access.

This role focuses on ensuring that all medical devices comply with international regulations while managing the technical documentation and communication with health authorities throughout the product lifecycle.

An amazing opportunity not to be missed !

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