Strategic Regulatory Affairs Lead — Medical Devices
bracco medical technologiesMinneapolis (MN)
Strategic Regulatory Affairs Lead — Medical Devices
Posted yesterday
bracco medical technologiesMinneapolis (MN)
SENIORITY
Manager
About the role
Bracco Medical Technologies is seeking a Principal Regulatory Affairs Specialist to develop and execute regulatory strategies for medical device products across lifecycle changes. You’ll lead global submissions and provide on‑site regulatory support for 510(k), EU MDR, and Health Canada efforts.
You will collaborate with cross‑functional teams, mentor staff, and oversee regulatory documentation, labeling review, and agency communications to ensure ongoing compliance and market access.
Before you apply
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Your profile is current
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Two examples you can talk through
Not a portfolio — just two pieces of work where you can explain the decisions and what you'd change.
A number in mind
What you're on now and what would make you move. We negotiate better when we know both.
Your notice period
Employers plan around it, and it's the question that stalls offers most often.
Once you apply, someone reads it and calls you before anything reaches the employer — usually within two working days.
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