Regulatory Affairs Specialist
Parisonsitemid
Posted 2 days ago · via Workday
About this role
At MiniMed, you can begin a lifelong career of exploration and innovation, while helping make a difference in the lives of people living with diabetes around the globe. You'll lead with purpose, breaking down barriers to innovation for a more connected, compassionate world. About the Role As a Regulatory Affairs & Quality Specialist, you will play a key role in supporting regulatory and quality activities across Benelux and France, ensuring compliance with EU and local regulations throughout the product lifecycle. Working closely with Competent Authorities, customers, tender organizations, and internal stakeholders, you will provide regulatory guidance, support field actions and post-market surveillance activities, and help drive compliance across the business.…
Read the full description on USA-Mini Med Distribution Corp.'s site →
What we'd score you on
reqspace match rubricFive dimensions, recruiter-grade. Upload your resume and we'll generate a written explanation of where you fit and where the gaps are.
1
Skills match
For this role: teams
2
Level fit
This role is mid-level. We check your trajectory against it.
3
Domain experience
Your work in the role's domain matters more than your years total. We weight recent and direct experience.
4
Recency
A skill you used last quarter weighs more than one from five years ago. We grade on recency, not lifetime.
5
Location fit
This role is based in Paris. We weight your proximity and willingness to relocate.
Score yourself on this role.
Free · no card · written explanation included
Skills in this role
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teams
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