Chargé d'affaires réglementair Dispositifs Médicaux - Sud Est
- Employer
- NonStop Consulting
- Location
- Marseille
- Salary
- Negotiable
- Closing date
- Apr 20, 2019
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- Sector
- Pharmaceutical, Regulatory Affairs
- Contract Type
- Employee
- Hours
- Full Time
- Organization Type
- Corporate
- Jobseeker Type
- Professional
Job Details
Missions :
En tant que consultant chargé des affaires réglementaires :
- Vous assurez l'élaboration, la constitution, le contrôle, le dépôt des dossiers de demandes de marquage CE auprès des organismes notifiés, leur renouvellement, des variations et des modifications dans le respect des procédures internes et de la réglementation en vigueur.
- Vous suivez l'avancement des dossiers auprès des organismes notifiés.
- De plus, vous assistez notre client dans le cadre des procédures (traductions, échange avec les autorités, traitement des spécificités…).
- Enfin, vous menez une veille réglementaire, scientifique et clinique.
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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