Unser Kunde ist ein führendes Schweizer Kosmetik.- & Care Unternehmen mit Sitz im Raum Zurich. Wir suchen ab sofort eine/n Manager/in im regulatorischen Bereich für ein 9 Monatiges Projekt mit der Möglichkeit der Verlängerung.

Projektstart: ASAP

Für unseren Kunden, einen internationalen key player im Bereich OTC, suchen wir per sofort oder nach Vereinbarung einen Account & Access Manager für die Zielgruppe Hospital/Spitäler in der deutschsprachigen Schweiz. Der Account und Access Manager ist ein fachlicher und kommerzieller Experte der die Spital-Strategie mit-entwickelt, anpasst und erfolgreich umsetzt.

Belle opportunité de rejoindre une équipe des affaires réglementaires sur des dispositifs médicaux innovants.

En tant que Responsable Amélioration Continue h/f, vous serez en charge du déploiements des outils Lean/6-sigma sur l'ensemble du site, et de la définition des projets liés. Poste basé sur Yverdon-les-Bains.

Develop and implement CH local market access strategies for existing products and localize global value dossiers for launch products to achieve a commercially successful market access environment. Executing value-price strategies in affiliates. Tailoring global payer value proposition and access strategy to local needs

My client is an independent and international pharmaceutical company located in Basel. They are currently looking for a Quality Assurance Manager to straighten their QA Team.

MDR 2017/745 Project Manager.

Innovative medical devices.

Our client is an International Biotech company located in Basel. Thanks to their constant growth we are looking for a talented Senior CMC Dossier Specialist to complete its CMC team.

As the Head of Quality Control m/f, your role will be to lead the Quality Control Team for activities related to the manufacturing of kits as well as QC methods development. You will report directly to the COO and collaborate closely with the Head of Production, the Industrialization Manager. Position based in Lausanne.

As Verification & Validation engineer, you will conduct equipment systems or software validations (IQ/OQ/PQ) for manufacturing and QC processes/equipment in the plant. Position based next to Lausanne.

I am currently supporting an international Biotech company who is currently creating a new position as CMC Dossier Manager as they are in constant growth.

The Associate Director of Medical Affairs Surgical primary responsibility is to develop and execute a comprehensive medical affairs plan that contributes to the achievement of the company's EMEA's short- and long-term goals. This position will closely collaborate with all relevant internal business partners ensuring that all medical initiatives and deliverables are aligned and integrated into the franchise brand plan.

I am currently supporting an international Biotech company who is currently creating a new position as CMC Dossier Specialist as they are in constant growth.

Clinical support of Hybrid surgical robot installation and increasing utilization procedures

This position reports to the Medical Manager Switzerland and Austria, but will work cross
functional with other department within region and global organisation.

MSL is a field-based professional who develop strong relationships with Medical Experts and members of the scientific community. They strategically prepare and support the development, launch and commercialisation of products through scientific exchange.

Great opportunity in Regulatory Affairs within an innovative medical device company.

Opportunité en tant que Chargé(e) d'Affaires Réglementaires au sein d'une entreprise internationale.

• This role will be responsible for execution of daily activities associated with implementation and maintenance of the QMS and QA activities in relation to Trading Entity Support the establishment of procedures and processes only
  Ensure all requirements to maintain the Wholesale Distribution Authorisation and appropriate licenses are met

As Manufacturing engineer m/f, you will be a main support to the Design Transfer project. Mission of 12 months.