Associate Regulatory Affairs Specialist at Medtronic | Torre
Associate Regulatory Affairs Specialist
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Medtronic

Associate Regulatory Affairs Specialist

Medtronic
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Full-time

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Remote (for Colombia residents)
Shared by
Laura Motta
 3 days ago

Responsibilities

We are hiring! Medtronic is looking for an Associate Regulatory Affairs Specialist to support medical device operations across LATAM & APAC.Key Responsibilities:Coordinate and compile documentation packages for regulatory submissions, license renewals, and audits.Maintain and organize regulatory records across document management systems.Support responses to regulatory agency requests and collaborate with cross-functional global teams.Requirements:Bachelor’s degree completed or in progress (Healthcare, Bioengineering, Biotechnology, Pharmacy, Business, or related).1–2 years of experience in Regulatory Affairs, Quality, Compliance, Documentation Management, or related operational areas.Fluent in English (professional working proficiency).Strong organizational skills with the ability to work independently in a remote setup.
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