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Sr. Regulatory Affairs Specialist - Medical Device
This person will be working with Quality, R&D, and regulatory to prepare and write regulatory submissions. With that, we need someone who has an understanding of quality and R&D as well as regulatory submissions, specifically understanding how design controls need to be applied. We need this person to be able to look critically at the regulatory documentation and understand if something is missing and if anything needs to be changed. This person will also manage device listings, registrations, licenses, and distribution authorizations.
This will be a great career growth opportunity to work in a small company environment and be exposed to a wide range of regulatory activities. If interested in learning more, please apply today!