Beschreibung

* Play a key role in bringing innovative medical technologies to market
* Collaborate with expert teams across product development and regulatory strategy

## About Our Client ##

Our client is a leading player in the medtech industry, known for its collaborative culture and commitment to innovation. The company operates across multiple product lines and markets.

## Job Description ##

* Contribute to the development and execution of product registration plans
* Identify and compile documentation for regulatory submissions
* Create submission dossiers and support external consultants/distributors
* Coordinate with internal teams to ensure timely and compliant registrations
* Manage product lifecycle changes and assess regulatory impact
* Define action plans for modifications, including validation testing
* Update registration files in line with evolving standards
* Provide regulatory guidance to internal and external stakeholders
* Support declaration of conformity and product presentation to authorities
* Collaborate with both product development and registration teams
* Participate in regulatory strategy during late design phases
* Ensure documentation complies with MDR and other relevant regulations

## The Successful Applicant ##

* Available immediately
* Experience in regulatory affairs within the medtech or medical device industry
* Strong understanding of MDR and technical documentation requirements
* Comfortable reading and interpreting complex technical files
* Curious and proactive about medical technologies
* Ability to work cross-functionally with development and registration teams
* Skilled in compiling and managing submission dossiers
* Excellent communication and coordination skills
* Detail-oriented with strong organizational abilities
* Capable of supporting both strategic and operational regulatory activities
* Fluent in English; French is a plus
* Team player with a collaborative mindset

## What's on Offer ##

* Opportunity to work on diverse and innovative medical technologies
* Dynamic and collaborative work environment
* Career development within a growing international company

Quote job ref

JN-092025-6831991

Job Function

Healthcare & Life Sciences

Specialisation

Regulatory Affairs

Industry

Healthcare / Pharmaceutical

Location

Geneva

Contract Type

Interim

Job Reference

JN-092025-6831991