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Regulatory Submissions Lead – FDA & eCTD Expert

Job in Bristol, Sullivan County, Tennessee, 37621, USA
Listing for: USAntibiotics, LLC
Full Time position
Listed on 2026-01-25
Job specializations:
  • Healthcare
    Medical Science Liaison
Job Description & How to Apply Below
A pharmaceutical company located in Tennessee is seeking a Regulatory Affairs Specialist to manage FDA submissions and ensure compliance with regulatory standards. The ideal candidate will hold a Bachelor's degree in a scientific discipline, have 3-5 years of regulatory experience, and demonstrate strong communication and organizational skills. Responsibilities include drafting submissions, coordinating with partners, and supporting interactions with regulatory agencies.

Occasional travel may be required.
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