RA/QA Specialist-Career Growth-Medical Devices-Paris, France

Location
Paris
Salary
€40000 - €45000 per annum
Posted
Dec 14, 2017
Closes
Jan 13, 2018
Ref
TG/59114/1
Contact
Tamanna Gandecha
Jobseeker Type
Professional
Organization Type
Corporate
Contract Type
Employee
Hours
Full Time

RA/QA Specialist-Career Growth-Medical Devices-Paris, France

This is a new exciting role within regulatory affairs and quality assurance to develop and grow your career in a leading medical device company. Our client are at an exciting point of growth, providing you with the perfect environment to growth at the same time on a global scale.

As the regulatory affairs and quality assurance specialist in this role your responsibilities will include but will not be limited to:

  • Working on the international registration process of class IIb and class III devices.
  • Play a crucial role across both regulatory affairs and quality assurance.
  • Assist in the management of the QMS.
  • Work closely with senior management to develop strategy and drive the department forward.

The ideal candidate for this role will have:

  • Several years of experience across both regulatory affairs and quality assurance.
  • Good knowledge within ISO 13485.
  • Any prior experience with higher risk devices would be a plus.
  • Fluency in both English and French are required.

Do not miss out on this great opportunity across both RA and QA; allowing you to develop your career.

Call me Tamanna Gandecha at NonStop Recruitment now for a confidential conversation. Contact me on regulatory@nonstop-devices.com or +41 435 0808 16, please send your CV in word format OR if this does not sound like the opportunity for you, but you are a regulatory affairs professional within the medical device industry, please feel free to get in touch, to see other opportunities we may have within this field.

NonStop is one of the largest and fastest growing specialised life sciences recruitment companies in Europe. We are proud members of the APSCo life sciences group who ensure we meet the highest quality standards within the recruitment industry. Our offices are located in the UK, Switzerland and the Czech Republic and we hold labour leasing licences across Europe. Please visit our website for a full list of the niche markets we cover.

What I offer: As a specialist Headhunter within regulatory affairs for the medical device industry I can offer: market knowledge and a personal service, therefore not just finding you suitable roles but in addition to this offering accurate and honest advice about salaries, work conditions and department reputations for positions across Switzerland.

KEY WORDS: regulatory affairs compliance, regulatory affairs, quality assurance, QMS, medical devices, france, regulatory affairs manager, quality management system, nonstop recruitment, medical device jobs