Regulatory Affairs Consultant-3-6 Month Project-Medical Devices

Regulatory Affairs Consultant-3-6 Month Project-Medical Devices-St. Gallen region, Switzerland

Rates: Dependant on experience

NonStop Medical Devices are exclusively working with a leading medical device company to hire a regulatory affairs freelancer to come on board for a 3-6 month project. Our client have a broad range of projects requiring the senior expertise of a regulatory affairs professional to assist with CE marking, documentation and the international registration process.

Our client are looking for consultants who are available with short notice to assist with documentation activities. You must be an experienced regulatory professional with specific experience within medical devices on an international scale. You will be fluent in both English and German.

We have project available work immediately so can get someone up and running with short notice.

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

NonStop is one of the largest and fastest growing specialised life sciences recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Switzerland and the Czech Republic and we hold labour leasing licences across Europe. Please visit our website for a full list of the niche markets we cover.

What I offer: As a specialist Headhunter within regulatory affairs for the medical device industry I can offer: market knowledge and a personal service, therefore not just finding you suitable roles but in addition to this offering accurate and honest advice about salaries, work conditions and department reputations for positions across Switzerland.

KEY WORDS: regulatory affairs consultant, FDA, PMA, 510K, american, medical devices, regulatory affairs manager, regulatory affairs expert, regulatory affairs specialist, nonstop medical devices, nonstop recruitment