Regulatory Affairs Manager / International Environment / Lugano

I am currently working with an established and well renowned company which is now looking to expand its regulatory team.

The position is very exciting since it will give the opporutunity to manager a portfolio of products from the pre approval to the post marketing authorization. It is a good opportunity to be autonomous and put to work the skills you acquired in the past. At the same time you will have the satisfaction to manage the whole process till the end and see for real the result of your own work.

The position will give you the chance to be heavily involved in scientific advice and HA meetings for EMA and FDA, giving you a strategic role in the company. In addition to this, there will be strategic input for due diligence and the likelihood of being involved with other early development projects.

Key Requirements:

• Over 5 years experience in regulatory affairs for clinical trials;
• Experience in scientific advice with health authorities ( EMA or FDA )
• Fluency in English
• Life Science degree

The position will require the full time presence of the candidate to the company offices located in Lugano.

If this job appeals to you please send me, Claudia De Veis, your most recent CV in Word format to C.Veis@nonstop-recruitment.com. If you are not interested but you can recommend someone in your network, do not hesitate to provide them with my details.

NonStop is one of the largest and fastest growing specialised life-sciences & Med-tech 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 for all EU8 countries. Please visit our website for a full list of the niche markets we cover.

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