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Project Manager MDR (Medical Device Regulation)
Eingestellt von Claremont Consulting Ltd
Gesuchte Skills: Client
Projektbeschreibung
My client a global organisation is seeking a Project Manager MDR (Medical Device Regulation) to join their team.
As the Project Manager (MDR) you will be responsible for ensuring the coordination of commercial work-streams related to the MDR impact on our product portfolio, from assessment till remediation. You will also act as primary link with the Global MDR Project Manager and the various functional leaders to ensure continuous marketability.
Key skills and experience
*Detailed experience as a Project Manager with MDR (Medical Device Regulation)
*Experience with regulatory/Business/Technical experience with demonstrated record of success in driving complex projects and decisions in the Medical Device environment. (Renal environment as a plus)
*Excellent ability to plan, prioritise and adapt to changes.
*Strong analytics and data management skills.
*Product marketability/Life cycle management experience.
*Stakeholder management experience.
As the Project Manager (MDR) you will be responsible for ensuring the coordination of commercial work-streams related to the MDR impact on our product portfolio, from assessment till remediation. You will also act as primary link with the Global MDR Project Manager and the various functional leaders to ensure continuous marketability.
Key skills and experience
*Detailed experience as a Project Manager with MDR (Medical Device Regulation)
*Experience with regulatory/Business/Technical experience with demonstrated record of success in driving complex projects and decisions in the Medical Device environment. (Renal environment as a plus)
*Excellent ability to plan, prioritise and adapt to changes.
*Strong analytics and data management skills.
*Product marketability/Life cycle management experience.
*Stakeholder management experience.
Projektdetails
Geforderte Qualifikationen
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Kategorie:
IT Entwicklung