Regulatory Affairs Specialist-Supportive Team-Neuchatel

£92472 - £96325 per annum
Aug 16, 2018
Sep 15, 2018
Tamanna Gandecha
Jobseeker Type
Organization Type
Contract Type
Full Time

Regulatory Affairs Specialist-Supportive Team-Medical Devices-Neuchatel, Switzerland

We spend more time with the people with work with than often our own friends circle. With this in mind, I have a fantastic role as a regulatory affairs specialist. You will join a supportive international team, where your career will develop successfully. Through the close-knit team you will lead an interesting working life as the team making the working day fun and exciting. No two days will be the same!

As the regulatory affairs specialist in this role your responsibilities will include but will not be limited to:

  • Working on key technical documentation files across both medical devices and cosmetics.
  • Handle the registration process on an international scale.
  • Working in cross-function teams, inclusive of quality and research.

The ideal candidate for this role will:

  • Have a strong background within regulatory affairs, with product experience within medical devices.
  • Quality experience or exposure would be a bonus for this role.
  • You will have worked on technical documentation and have a key understanding of the international standards.
  • You will be fluent in English and French or German.

Do not miss out on the great opportunity to join a supportive team that will encourage your career in regulatory affairs.

Call me Tamanna Gandecha at NonStop Recruitment now for a confidential conversation. Contact me on 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 specialist, regulatory affairs manager, senior regulatory affairs specialist, medical devices, regulatory affairs, switzerland, FDA, 510K, nonstop recruitment, registration, quality assurance, cosmetics