- VaudPermanent
Following the promising clinical results achieved with its CE mark device, the company has raised funds for developing its commercial operations and is now actively looking for an experienced Sales Director to build-up entirely a new business.
Innovative growing company in medical equipment
Entrepreneurial role with strong impact for the company
View Job - VaudTemporary
Dans le but de renforcer sa Sales Team, notre client est à la recherche d'un/e Délégué/e Médical/e pour la région de VD / NE / JU / FR.
Travailler pour une entreprise biopharmaceutique
Intégrer une équipe de collaborateurs motivés et orientés vers le succès
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In order to strengthen its commercial activities, our client is looking to expend its sales team and recruit a Sales Representative to lead the Vaud canton.
Leader on the European market for medical diagnostics
Dynamic Sales team in full expansion
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The Senior Director will be responsible for managing all aspects of operational plans across a program with multiple global clinical trials and serve as a leader to the clinical operations team and a key member of the clinical development department. The position will report to the Head of Global Clinical Operations based in the US.
Fast growing start-up organization
Leadership role
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Prepare and coordinate various activities to make applications for product licenses.
Great opportunity to join a market leader in medical device.
International exposure.
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The Regulatory CMC Specialist is responsible for preparing and updating the CMC sections of assigned products (Rx and OTC drugs). Support the RA Managers for regulatory strategy of development and commercial products.
International company
Large product portfolio
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Manages Regulatory Affairs activities for all new and existing product development, including development of regulatory requirements/strategies.
Software products - Class IIb
Global role
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The Clinical will assume a leadership role in overseeing the design, implementation, conduct and evaluation of oncology clinical trials to ensure data quality and integrity.
Fast growing start-up organization
Innovative drug development
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Our client is looking for a Technical Documentation Coordinator to support its regulatory affairs team.
Great opportunity to join a market leader in medical device
To be part of the regulatory affairs team
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Global scope of activities.
Fast growing company.Global scope of activities
Fast growing company
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The Regulatory Affairs lead will have to manage CE Mark approvals and geographical expansion while managing a small team of RA Specialists.
Global Company
Multi-tasking working environment
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The incumbent will be responsible for EMEA quality and regulatory strategies in support of consumer goods business (Oral Care Company) for drugs, medical devices, cosmetic products, foods/food supplements and commodity products.
Our client is a healthcare company with its EMEA headquarters based in Romandie
Management of a large product portfolio
Save Job View Job - MorgesPermanent
Oversee and support the requirements related to the EMEIA tender process, support the global regulatory intelligence and regulatory surveillance processes, advocacy with government bodies and manufacturer associations across Europe, implementation of new regulation, tender management.
Innovative Medical Company
Dynamic environment
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To accompany the strong growth of the company, our client is looking to strengthen its clinical team and is looking for a Global Clinical Research Specialist.
Major Company in the Dental Industry
Join a dynamic team for new product launch
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