Global Regulatory Strategist – Medical Devices
Listed on 2026-10-10
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Pharmaceutical
Healthcare Compliance, Regulatory Compliance Specialist
ELITechGroup is seeking a Regulatory Affairs Specialist to ensure products comply with global regulatory requirements throughout development, registration, and post-market activities. You will prepare submissions (FDA/CE), interpret applicable regulations, and support cross-functional teams across R&D, Quality, and Marketing.
The role emphasizes collaboration, documentation, and ongoing regulatory monitoring to align with business objectives while maintaining compliance across multiple markets.
This role is for the Global Regulatory Strategist – Medical Devices role at ELITechGroup.
The position is based in Logan, UT, United States.
This opportunity is part of our work in Bio & Pharmacology & Health, Management & Operations.
The advertised compensation is 65.000 - 95.000.
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
Learn more about the Global Regulatory Strategist – Medical Devices role in the description above.
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