Project Manager – MDR Project (Medical Devices)
Hybrid Working | Contract until Early 2026 |
Full-Time | Competitive Hourly Rate | Early June Start
The Role:
We’re partnering with a leading global medical device company on a mission to bring a next-generation device to market, with CE certification under MDR.
With a skilled R&D team and a technically ready device, they now need an experienced Project Manager to lead documentation and delivery.
This is a high-impact role at the intersection of technical, regulatory, and global collaboration - ideal for someone who thrives on structure, momentum, and stakeholder engagement.
What’s the challenge?
You’ll drive the preparation and structuring of the MDR Technical File, owning the end-to-end process across internal teams and contract manufacturers in Europe and APAC.
You’ll set timelines, define and defend strategy, and keep engineers, RA/QA, and leadership aligned and accountable.
What you’ll be doing:
- Lead the CE certification project under MDR
- Define and drive strategy, timelines, and stakeholder engagement
- Coordinate activities across three international locations
- Communicate clearly and assertively with internal and external teams
- Summarise project status and risks for senior leadership
What we’re looking for:
- Proven track record leading medical device development and certification projects
- Strong understanding of MDR requirements and Technical File structure
- Exceptional project leadership — assertive, organised, and empathetic
- Experience coordinating multi-site, international teams
- Strong stakeholder management and strategic communication skills
- Background in RA/QA, R&D, or regulatory documentation is a strong plus
Sound like your kind of challenge?
This position is moving quickly to interview and offer. Apply now with your CV or message me directly to learn more.
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- Posted
- May 26, 2025
- Type
- Contract
- Level
- Mid-Senior
- Location
- Flemish Region
- Company
- Connect Life Science
Industries
Categories
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2026-06-13
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