Regulatory Project Manager - MDR transition
11.06.2019 | Employee | 100%

1 year temporary project management position related to the MDR transition

Regulatory Project Manager - MDR transition

International medical device company

Description

  • Crossfunction role to coordinate the RA resources related to the MDR transition
  • Works internally with different key stakeholders in Europe and in the USA : RA, QA, R&D..
  • To coordinate RA stakeholders to ensure deadlines are met on a timely manner
  • To work on submissions and life cycle management activities.

Profile

  • Previous significative experience in Regulatory Affairs in a pharmaceutical/medical device environment
  • Experience in combination products would be a plus
  • PMP certification would be a plus
  • Fluent in English
  • Must be detail oriented with good organizational skills with the ability to analyse regulatory documents

Job Offer

Project managament related to the MDR transition

11.06.2019
Employee, 100%

Contact

Michael Page Switzerland
Quai de la Poste 12 1204 Geneva
1204 Nyon
Michael Page
Quai de la Poste 12
Genève

Industry

Human resources / Personnel services
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