Regulatory Affairs Specialist - Medical Devices - France
- Employer
- NonStop Consulting
- Location
- Antibes
- Salary
- Negotiable
- Closing date
- May 19, 2019
View more
- Sector
- Pharmaceutical, Regulatory Affairs
- Contract Type
- Employee
- Hours
- Full Time
- Organization Type
- Corporate
- Jobseeker Type
- Professional
Job Details
Your main responsibilities will include:
· Work with the product team to develop regulatory strategies for the approval of new medical
devices or their changes.
· Determine and communicate to the teams of R&D / Industrialization / Validation, regulatory
requirements for the development and registration of new products, and provide the
appropriate procedures
· Handle the risk management process of the projects
· Check the conformity of the DHF and DMR.
· Check the technical documents related to the products changes, including changes of
processes and materials.
· Assess the impact of the new technical standards and regulations, and participate in the
implementation of the actions.
· Ensure continuous improvement of the process in its areas of expertise
· Support the export registration team
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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