Regulatory Affairs Specialist-Class III products-Geneva, Suisse
Regulatory Affairs Specialist-Class III products-Geneva, Switzerland
With the changing regulations next year, NonStop Medical devices has a fantastic role that will give you the opportunity to work on the registration of innovative class III devices. On behalf of our market leading client, we are searching for a regulatory affairs specialists to join a close knit team on to work on international projects. This is a great opportunity to progress your career into high risk products and work alongside some of the top experts in the industry.
The manager which you will report into is supportive and encouraging, where they will be willing to put time into training you within the full product life cycle of medical devices. This will allow you to develop your career in a supportive environment and gain invaluable expertise within CE marking, technical documentation and the registration process.
The ideal candidate: You will come from a strong scientific or engineering background within the medical field. You will have a few years of experience within regulatory affairs and worked on the registration process. Any previous experience of working with class III devices would be an advantage for this role. You will speak fluent English an advantage.
Do not miss out on the opportunity to advance your regulatory affairs career within the higher risk and innovative medical devices.
Call me Tamanna Gandecha at NonStop Recruitment now for a confidential conversation. Contact me on firstname.lastname@example.org or +41 435 0808 16, please send your CV in word format OR if this does not sound like the opportunity for you, but you are a regulatory affairs professional within the medical device industry, please feel free to get in touch, to see other opportunities we may have within this field.
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