Exigences

Niveau d'étude requis
Bachelor / HES
Expérience requise
Entre 1 et 3 ans
Connaissances linguistiques requises
anglais

Détails

Lieu
Zug
Horaires de travail
Temps plein
Secteur
Technique médicale
Professions
Pharmaceutique

Description

Become a Key member of the RA team helping clearing advertising and promotional material.

Client Details

Our client is a global market leader in the Medical Devices arena. Globally over 20 million people depend on our client devices to lead a healthier life.

Description

This role is part of the Global Copy Clearance Team, responsible for Advertising and Promotional Copy review, reporting into Global Regulatory Affairs.

  • Manage the routing, processing and storage of promotional content and claims submissions to ensure quality and cycle time goals are met.
  • Review claims and copy submissions in the Zinc MAPS Electronic Copy Review System to confirm that the necessary documentation is available, prior to distribution to reviewers.
  • Assist Originators with fulfilling the submission requirements, as needed.
  • Inform Copy Review Manager about unresolved issues between copy originators and reviewers to ensure that issues are resolved in a timely manner and changes are implemented as requested.
  • Ensure completed, approved submissions match final artwork.
  • Identify areas for process improvement and drive implementation.
  • Ensure that copy review submissions are stored in alignment with defined standards and documentation requirements.
  • Train Copy originators / Users on Copy Clearance process and the Zinc MAPS Electronic Copy Review System (via Conference Calls and WebEx).
  • Develop and maintain training / guidance materials.
  • Align target review cycle times/responsiveness goals with Copy Review Manager.
  • Work towards efficient review cycle.

Profile

  • Bachelor or Master degree
  • Minimum 3 years of work experience (at least 1 year of this time in a regulated environment, e.g. Pharma or Medical Devices).
  • Background in Marketing, Communication, Regulatory Affairs, Legal will be an asset.
  • Fluent in English (Knowledge in another European language is beneficial).
  • Accuracy with attention to detail.
  • Comfortable with working in multi-disciplinary teams in an international, culturally diverse environment.
  • Good project management skills.
  • Strong communication skills.
  • Comfortable working in a process-driven, regulated environment.

Job Offer

Help people around the globe leading a healthier life.

Join a global player in the Medical Devices arena.

Competitive Salary Package.

Michael Page
Non disponible

Informations de contact

Michael Page
Oliver Daidone
07g
Non disponible