Regulatory Affairs Lead - Medical Devices Submissions
Listed on 2026-10-17
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Healthcare
Healthcare Compliance, Medical Science Liaison
Highridge Medical seeks a Regulatory Affairs Senior Specialist to lead regulatory activities for key brands, guiding strategies from product concept to international submissions. You will collaborate with development teams to ensure compliant documentation and registration across markets.
The ideal candidate has strong writing skills, a track record in submissions, and at least 5–7 years in regulatory affairs or related fields within the medical device sector.
Step into the Regulatory Affairs Lead - Medical Devices Submissions role at HIGHRIDGE Inc. in Westminster, CO, United States and grow with us.
The position is based in Westminster, CO, United States.
This opportunity is part of our work in Finance, Bio & Pharmacology & Health.
The advertised compensation is 85..
We aim to respond to suitable candidates as soon as possible.
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