- 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
- VaudPermanent
In order to support our client business development, we are looking for a Tender Submission Specialist that will design, implement and execute the process to answer tenders and RFP.
Involving within a faced paced growing environment
Work with a cross functional team approach and spirit
- VaudPermanent
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
- LausannePermanent
We are looking for an Intellectual Property Associate.
Growing Biotech Company
Intellectual Property - One Year contract
- 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
- NyonPermanent
Prepare and coordinate various activities to make applications for product licenses.
Great opportunity to join a market leader in medical device.
To be part of the regulatory affairs team.
- NyonPermanent
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 support the regulatory affairs team
- NyonPermanent
The Clinical Affairs Manager will be responsible for successful execution of assigned clinical field trials within budget and in conformance with global regulations and internal policies and procedures.
Mid-Sized organization
Global responsibilities
- MorgesPermanent
Regulatory registrations/filings, Regulatory operations support, Quality Management System implementation & coordination.
Fast growing company
Innovative Medical Technology
- LausannePermanent
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
- NyonPermanent
The incumbent provides administrative expertise in receipt, processing, monitoring and reporting of product defect complaints, serving as primary contact.Innovative medical technology
International exposure
- VaudPermanent
An innovative, entrepreneurial life science company operating in the fields of nutrition and drug discovery is recruiting a
Director of Regulatory Affairs and Quality AssuranceInnovative and entrepreuneurial Life Science company
Position with high responsibilities
- MorgesPermanent
The Regulatory Specialist supports the department by evaluating medical device changes, determining and executing registration strategy and ensuring compliance of marketing material.Fast growing company
Innovative Medical Technology
- LausannePermanent
In order to lead major projects following the development of the product portfolio, our client is looking for a Regulatory Affairs Project Manager.
Global leader in the dental industry
Global experienced Regulatory Affairs project Manager
- LausannePermanent
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
- VaudPermanent
As a Regulatory Affairs Technical File Specialist, you lead actions to develop the technical files system according the latest regulations and requirements.
You're an experienced Quality System / Regulatory Compliance engineer
A multicultural company who is leader on its market
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