Regulatory Affairs Manager - Devices - Prague

My client, a medical devices manufacturer and global player in their field is currently looking for a manager in Regulatory Affairs for a fantastic opportunity based in Prague in the Czech Republic. 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 high risk products across all different areas.

As the Regulatory Affairs Manager, this is a role where you would be the handling most Regulatory activities. This position will mainly be focused on product registrations mainly in the CIS, MENA and EU regions.

Successful Candidates will have:

• 3+ years minimum experience in Regulatory Affairs for Medical Devices
• Solid Regulatory Affairs background with submissions to CIS and MENA Countries
• Familiarity with ISO 13485, 21 CFR Part 820 QSR, and Medical Device Directives (MDD)
• Speak fluent English

If you are a Regulatory Affairs professional with over 3 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: Prague

Contact: Mahdi Chab

Email: m.chab@nonstop-recruitment.com

Tel No: +44 207 940 2105

Keywords: Manager, Quality Assurance, Regulatory affairs, quality assurance, medical devices, produktzulassung, regulatory affairs medizinprodukten, FDA, Prague, Czech Republic, Devices, CIS, EMEA, EEMEA, Russia, Middle East, Czech, Praha.