Project manager medical device regulation

15-2-2019 braine-l'alleud
description de la société

Our client pursues one and the same goal: to help save and preserve lives around the world.

description de la fonction

Do you have experience as Project manager in medical device regulation and RA?

Contact me :

Ensure to coordination of the commercial work-streams related to the Medical Device Regulation impact on our product portfolio, from assessment till remediation.

Collaborate and act as primary link with the Global MDR Project Manager and the various functional leaders to ensure continuous marketability.

Manage the portfolio analytics in the context of MDR, by maintaining and analysing data in order to proactively flag any market risk/issue.

Drive awareness and dedicated communication, reporting KPI’s to Global Marketing Senior Management.

vos atouts

At least 7 to 10 years experience in Project Management, more specifically related to either Regulatory Affairs or Medical Devices.

Highlight is on Product marketability / Life cycle management experience, with RA & Med Device as a background.

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)

Strong leadership and interpersonal skills and excellent communication across functions, organizational levels and cultures to help deliver results.

Excellent ability to plan, prioritize and adapt along changes.

Strong analytics and data management skills.

English fluent, French or any other Eu language as a plus


We offer an attractive salary with extra-legal advantages :
- Group insurance
- Hospitalisation insurance
- Meal vouchers of 7 euros gross per working day
- Reimbursement km or company car
- Monthly allowance (50 euros net per month)
- A 13th month
- Training
- Etc.
A rate as freelance is also possible.

ingénieur (m/f)
type de job
temps plein
type contrat
missions à long terme
informations de contact
Charlotte D'Hont