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Regulatory Affairs Specialist

Posted on Jan 17, 2020 by NES IT

Zürich, Switzerland
Research
16 Feb 2020
Annual Salary
Contract/Project
I am collaborating with a leading international Medical Device company who are looking to add a Regulatory Affairs Specialist to their Regulatoryy team to preapre them for the arrival of the new MDR, MDSAP audit programme and FDA inspections. This is an exciting opportunity for an experienced consultant to work for an organisation that is growing rapidly and enabling people around the world improve one of their vital senses.

My client is looking for an individual who has knowledge of post market surveillance aswell as well change management. Someone who is dynamic, agile and dedicated to the task in hand.

Key Requirements:

-2+ years regulatory affairs experience in Medical Devices (Preferebly class I + IIa)
-Fluency in English, (German Desirable)
-Degree in related field
-PMS and change management

If this role is of interest to you and you would like to learn more please contact me:

Email - (see below)

Established in 1978, NES Global Talent provides a complete range of contract and permanent talent solutions to the Oil and Gas, Power, Construction and Infrastructure, Life Sciences, Manufacturing and IT sectors worldwide. With more than 40 offices in 28 countries, we are able to provide our clients with the engineering and technical expertise they need, wherever and whenever it is needed. Offering far more than a traditional recruitment service, we fully support our contractors while they are on assignment with everything from securing visas and work permits, to providing market leading benefits packages and accommodation, ensuring they are safely and compliantly able to support our clients.

Reference: 829452716

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