Regulatory Affairs Specialist - Diagnostics
- Employer
- NonStop Consulting
- Location
- Copenhagen
- Salary
- €60000 - €80000 per annum
- Closing date
- Sep 17, 2016
View more
- Sector
- Pharmaceutical, Regulatory Affairs
- Contract Type
- Employee
- Hours
- Full Time
- Organization Type
- Clinical Practice
- Jobseeker Type
- Professional
Job Details
My client, a medical devices manufacturer and global player in their field is currently looking for a specialist in Regulatory Affairs for a fantastic opportunity based in Copenhagen, Denmark. This is a fantastic Regulatory Affairs opportunity for someone who is looking for a change in their career whilst working for a leading company in the in the innovative field of innovative products mainly within the diagnostics field.
As the Regulatory Affairs Specialist, this is a role where you would be the handling most Regulatory activities. This position will mainly be focused on product registrations on a global level but mainly EU CE marking, FDA and APAC.
Successful Candidates will have:
- 2+ years minimum experience in IVD in Regulatory Affairs or Quality Assurance
- Solid Regulatory Affairs background with submissions to EU & FDA
- Familiarity with ISO 13485, 21 CFR Part 820 QSR, and Medical Device Directives (MDD)
- Speak fluent English (Danish is a bonus)
If you are a Regulatory Affairs professional with over 2 years experience and you speak fluent English then please contact me, Mahdi Chab of NonStop Recruitment with the contact details below or alternatively please send me a copy of your Word CV by email to apply!
If this does not sound like the opportunity for you, but you are a regulatory affairs or Quality Assurance professional within the medical device industry, please feel free to get in touch, to see other opportunities we may have within this field.
Location: Denmark
Contact: Mahdi Chab
Email: m.chab@nonstop-recruitment.com
Tel No: +49 8921 0933 64
Keywords: Manager, Quality Assurance, Regulatory affairs, Zulassungs, quality management, quality assurance, medical devices, produktzulassung, regulatory affairs medizinprodukten, FDA, Malmo, Denmark, Copenhagen, Nordics, Sweden, Devices
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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