Beschreibung

* Gain valuable experience in a globally recognized healthcare company
* Develop your regulatory expertise through hands-on experience

## About Our Client ##

Our client a healthcare company in Geneva.

## Job Description ##

* Support the Regulatory Affairs team in the preparation, submission, and tracking of regulatory documents.
* Coordinate with internal departments (Quality, Clinical, R&D, Marketing) to gather necessary documentation.
* Maintain regulatory databases and ensure timely updates of product information.
* Assist in compiling dossiers for product registrations, renewals, and variations in compliance with Swissmedic and EU regulations.
* Monitor regulatory timelines and ensure adherence to submission deadlines.
* Liaise with health authorities and third-party partners as needed.
* Ensure compliance with internal SOPs and applicable regulatory requirements.

## The Successful Applicant ##

* Bachelor's degree in Life Sciences, Pharmacy, or a related field.
* Minimum 2 years of experience in Regulatory Affairs within the healthcare, pharmaceutical, or medical device industry.
* Familiarity with Swiss and EU regulatory frameworks.
* Strong organizational and communication skills.
* Proficiency in Microsoft Office and regulatory tracking tools.
* Fluent in English; French is a strong asset.

## What's on Offer ##

* A collaborative and supportive team environment.
* Exposure to international regulatory processes.
* Opportunity to work with a reputable healthcare company in Geneva.
* Competitive compensation through Michael Page.

Quote job ref

JN-062025-6759061

Job Function

Healthcare & Life Sciences

Specialisation

Regulatory Affairs

Industry

Healthcare / Pharmaceutical

Location

Geneva

Contract Type

Interim

Job Reference

JN-062025-6759061