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Regulatory Affairs Specialist - Devices - Brand New Role

Employer
NonStop Consulting
Location
München (81249)
Salary
€60000 - €80000 per annum + Bonus
Closing date
Jan 7, 2017

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Sector
Pharmaceutical, Regulatory Affairs
Contract Type
Employee
Hours
Full Time
Organization Type
Clinical Practice
Jobseeker Type
Professional

Job Details

My client, an internationally successful and globally known medical devices company, is looking for Regulatory Affairs Specialist to join their function near the beautiful city of Munich.

This is a Regulatory Affairs opportunity for someone who is looking to work for a smaller company where your work is of higher value, there is more chance of career progression once the business grows, AND you are more independent in the way you work. Furthermore this firm guarantees longevity and a positive working environment.

As the Regulatory Affairs Specialist, this is a role where you would be supporting most Regulatory activities. This position will mainly be focused on pre-market work and reviewing documentation.

Successful Candidates will have:

  • 2+ years minimum experience in medical device 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 and German

If you are a Regulatory Affairs professional with over a years experience and you speak fluent English and German 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: Munich

Contact: Mahdi Chab

Email: m.chab@nonstop-recruitment.com

Tel No: +49 8921 0933 64

Keywords: Specialist, Associate, Regulatory affairs, Zulassungs, quality management, quality assurance, medical devices, produktzulassung, regulatory affairs medizinprodukten, FDA, Frankfurt, Munich, Bayern, Bavaria, Muenchen, Deutschland, Germany, 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. 

Company info
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