Regulatory Affairs Manager in Rotkreuz

veröffentlicht:
Ort
Rotkreuz, Zug
Sektor
Life Sciences
Jobtyp
Contract
Referenznummer
8861
Kontakt
Megann Löffler, Basel Professionals IT & Life Sciences
Telefon
058 201 55 50
Jetzt bewerben

Stellenbeschreibung

For our client in Rotkreuz, a Leader in the pharmaceutical industry, we’re actively looking for a : 

Regulatory Affairs Manager

Location: Rotkreuz, Switzerland
Duration: Until 31/12/2017 (with option of extension)
Start date : asap
Full time position (100%)

 

Job description : 

  • Project Lead Regulatory, within the scope of a project for new products or during the product life cycle :
  • Provide regulatory support to the R&D Project teams with the applicable Design Control processes
  • Responsible for the  qualification and classification of the development object and related submission strategy;
  • Interface with the correspondent RA-FL for submission strategies, planning and support;
  • Escalate project related regulatory issues;
  • Review of labeling
  • Assemble the documents and the project deliverable (or coordinate the activities) for the preparation of - world-wide registration and resolution of possible conflicts.
  • Administration of Product declarations, Certificates and other, similar documents

Your Profile : 

  • Support of IVD instrument development and life cycle management of product registrations
  • Regulatory/Design Quality for several years for IVD or Medical Devices preferred for Software and instruments
  • 5 years experience in Medical Device or IVD industry
  • University Degree
  • English spoken and written 

We are looking forward to receiving within your application:

•    your CV in English
•    latest Work Certificates
•    the date of your availability

Apply now to be considered – Good to know you!

For more information and your application, please contact:    

Megann Löffler
Professionals Life Sciences Recruiter
Randstad (Suisse) SA

Jetzt bewerben