Regulatory Affairs Specialist-FDA Focus-Medical Devices-Germany

Regulatory Affairs Specialist-FDA Focus-Medical Devices-Tuttlingen-Germany

Gain an opportunity to be the next regulatory affairs specialist with our market leading client based in Tuttlingen. This is a great opportunity to develop your career on an international scale and become a key expert with the FDA registration process. If you are an experienced regulatory affairs professional within the medical device industry, looking to develop global expertise ensure you apply now!

As the regulatory affairs specialist in this role your responsibilities will include but will not be limited to, working on the global registration process of class III devices, with specific regards to implantable. You will work on full product life cycle management, working on clinical and post-marketing registrations. Due to the global nature of the role you will work closely with local authorities and the FDA.

The ideal candidate for this role will:

• Come from a strong regulatory affairs background from the medical device sector.
• You will have worked with class III devices.
• Have strong knowledge of ISO 13485 and 510K.
• You will be fluent in both English and German.

Apply now to find out more about this regulatory affairs specialist role with a market leading medical device company and gain a global role today.

Call me Tamanna Gandecha at NonStop Recruitment now for a confidential conversation. Contact me on regulatory@nonstop-pharma.com 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.

KEY WORDS: regulatory affairs specialist, regulatory affairs, regulatory affairs associate, quality assurance, medical devices, france, registration, ISO 13485, medical device jobs, nonstop recruitment, french jobs