Regulatory Affairs Specialist - Swiss Med Tech - English/German/French - Diagnostic products
Based in Central Switzerland, our client develops, manufactures, and sells products and services for the Bioscience, Diagnostic, and Hospital sectors, globally.
A fabulous opportunity has just arisen to join as a Regulatory Affairs Specialist, with tasks to include the preparation and submission of applications to international regulatory authorities for product and change approvals, provide regulatory inputs to product development projects, develop regulatory strategies for changes and new products worldwide, and lead and coordinate regulatory projects and compliance initiatives as required.
If you have a higher degree in a legal, science or engineering discipline with previous medical device regulatory experience, then please do apply. This is a fabulous young company with big plans and many opportunities to offer.
English is the corporate language, and with German and French both beneficial.
For more information on this vacancy, or any other opportunities within the Swiss Medical Devices sector, please contact the Senior Consultant Andrew Boroky by applying with your resume in WORD format, plus scanned copies of training certifications and ArbeitsZeugnisse (work references).
Keywords: Regulatory Affairs, product licence, registration, regulatory agency inspections,complaints, vigilance, diagnostics, medical devices, Switzerland, post market surveillance, German, English, French, manufacturing, Research & Development, CE Mark, FDA, Nonstop Consulting
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 Switzerland, Luxembourg, the Czech Republic, UK, Romania, and the USA, and we hold labour leasing licences across Europe. Please visit our website for a full list of the niche markets we cover