2 x Regulatory Affairs Specialists - Devices - Brand New Roles

München (81249)
€60000 - €70000 per annum + Bonus
Sep 23, 2016
Oct 23, 2016
Mahdi Chab
Jobseeker Type
Organization Type
Clinical Practice
Contract Type
Full Time

My client, an internationally successful medical devices company who work in the respiratory/cardio field, are 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 you work is of higher value, there is more chance of career progression once the business grows, AND you are more independant in the way you work. Furthermore the emphasis on TEAMWORK in this company is OUTSTANDING.

As the Regulatory Affairs Manager, this is a role where you would be supporting most Regulatory activities. This position will mainly be focused on pre market work but there will also be post market work in the future.

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: Manager, Quality Assurance, Regulatory affairs, Zulassungs, quality management, quality assurance, medical devices, produktzulassung, regulatory affairs medizinprodukten, FDA, Frankfurt, Wiesbaden, Budenheim, Frankfurt, Deutschland, Germany, Devices

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