Regulatory Affairs Manager - Medical Devices
- Employer
- NonStop Consulting
- Location
- Zürich
- Salary
- Negotiable
- Closing date
- Jan 5, 2019
View more
- Sector
- Pharmaceutical, Regulatory Affairs
- Contract Type
- Employee
- Hours
- Full Time
- Organization Type
- Corporate
- Jobseeker Type
- Professional
Job Details
Your Qualifications
* Master's degree in scientific discipline such as biology, chemistry, engineering or equivalent
* 5 - 10 years' experience in general regulatory affairs, with at least 4 years of international
regulatory experience
* Profound experience with international medical device (class II & III) regulatory approvals and
submissions
* In depth knowledge on the new MDR and on all international regulations
* Familiar with the medical device and combination device European regulations (93/42/CE and
2001/83/CE)
* Strong understanding of international regulatory landscape & required approaches and strategies
* Agility to handle and deliver on a multitude of projects, programs, and priorities paired with high
sense for execution and teamwork
* Collaborative, empathic and solution-oriented individual
* Excellent command of spoken and written English and German, any other language is an asset
Company
Our Consultants are trained to deliver an exceptional standard of recruitment services to clients across the life sciences, chemical, care, educations, technical, digital and finance industries.
Our clients – and bottom line profits - tell us that we do a great many things very well. Complacency, however, is the last word you would associate with us. We work incredibly hard to deliver better and better results, based on stronger and stronger service delivery. Which is why we believe the best is yet to come – for us, our clients and for the people who have what it takes to join us on the journey.
The result? We’re expanding (in the UK and across Europe and even to Boston, US) and continue to post impressive performances in all our niche sectors.
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