Responsable Affaires Réglementaires - Suisse
- Employer
- NonStop Consulting
- Location
- Paris
- Salary
- Negotiable
- Closing date
- Nov 17, 2017
View more
- Sector
- Pharmaceutical, Regulatory Affairs
- Contract Type
- Employee
- Hours
- Full Time
- Organization Type
- Corporate
Job Details
Responsable Affaires Réglementaires - CDI
Laboratoire innovant en Suisse francophoneMissions principales
- Veiller à l'obtention/suivi des A.M.M, leur modification, leur renouvellement en procédures nationales, européennes (MRP, DCP et centralisée)
- Participer aux inspections des Autorités de Santé et audits internes/externes rattachés aux Affaires Réglementaires.
- Répondre aux exigences et aux questions des Autorités de Santé françaises dans les délais convenus ; représenter Takeda France auprès de ces instances.
- Libérer les documents promotionnels sur délégation du PR
- Superviser la veille réglementaire, en informer les services concerné.
- Bac+5 Life Sciences
- Expérience significative en CMC sur produits Biologics
Demander à joindre le département Affaires Réglementaires France au 01 76 75 33 40
ou Envoyer votre CV à l'adresse suivante : h.djilali@nonstop-pharma.com
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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