Regulatory Affairs Specialist

I am partnering an international Medical Device organisation based in Yorkshire to find a Regulatory Affairs Specialist to lead them in the most efficient way to achieve accreditation for their products in the global market, to drive the companys transition to the new European regulations and act as the main point of contact for Regulatory Affairs across the business.
The company is known for its longstanding commitment to innovation and dedicate extensive resource to the development of disruptive technology to improve the lives of patients around the world.
The position is based in Yorkshire and is offering a competitive package.
The successful Regulatory Affairs Specialist must have:

At least 5 years of experience in a Regulatory position in the Medical Device industry
Working knowledge of the regulatory requirements for Class III Medical Devices
Experience creating and submitting Technical Files and specific Design Dossiers on a global scale (North America, LATAM and APAC are desirable)
If this is the opportunity that could take your career to the next level, apply now!

Sthree UK is acting as an Employment Agency in relation to this vacancy. Advertised through Zoek Advertised through Zoek 42942.