Offres d'emploi Santé Sciences De La Vie - Suisse

Our client is an innovative biotechnology startup company focused on the development of cutting-edge biologics to address high unmet medical needs. With a highly experienced leadership team and promising pipeline, the company is entering late-stage preclinical development and preparing for regulatory submission.

Our client is seeking a Regulatory Affairs Specialist to support product registration and lifecycle management in the medtech sector. You will be responsible for compiling technical documentation and ensuring regulatory compliance throughout the product journey.

As a Medical Sales Representative in Switzerland, you will play a key role in driving growth, promoting clinically validated solutions, and building long-term partnerships with health-care providers. You'll serve as the primary point of contact for dental professionals and sleep specialists, ensuring a high standard of technical and commercial support. The position reports to the Regional Director for the DA CH region

Our client, a globally leading pharmaceutical company, is currently seeking a Logistics Specialist - Cold Chain for the Lucerne area. The role starts as soon as possible and is offered as a 6-month temporary contract with a hybrid working model.

The role involves leading a small commercial team, developing distributor and B2B healthcare partnerships, and driving international growth in a fast-scaling environment.

Our client is a leading pharmaceutical company looking for a highly organized and motivated individual to join their Medical Affairs team as Project Management. This role provides essential administrative and operational support for strategic key opinion leader (KOL) engagements, and digital initiatives. The successful candidate will ensure smooth project execution and play a key role in driving the success of Medical Affairs initiatives.

We are seeking a highly organized and detail-oriented Regulatory Affairs Coordinator to join a leading healthcare company in Geneva. This is a 12-month assignment managed through Michael Page, offering a unique opportunity to contribute to regulatory operations in a dynamic and international environment.

Au sein du département Qualité, assurer l'enregistrement des produits, de leur conception à leur distribution, et leur conformité aux normes réglementaires.

Dans un contexte de forte croissance, notre client - acteur reconnu du secteur médical - renforce sa structure Business Development. Rattaché(e) à la Direction Générale, le ou la future titulaire du poste interviendra principalement en support sur les projets de Licensing-in, avec une évolution possible vers davantage de proactivité.