Regulatory Affairs Manager — FDA Submissions & Compliance
1100 mylan pharmaceuticalsWashington, DC
Regulatory Affairs Manager — FDA Submissions & Compliance
L7
1100 mylan pharmaceuticalsWashington, DCyesterday
Industries
Electromedical and Electrotherapeutic Apparatus ManufacturingPharmaceutical Preparation ManufacturingBiological Product (except Diagnostic) ManufacturingViatris in Washington, DC, seeks a Manager, Regulatory Affairs to lead regulatory submissions (IND, NDA, ANDA) and ensure FDA compliance across development, manufacturing and QA. You will coordinate with QA, QC, Manufacturing, R&D and other groups to assemble documentation and respond to agency requests.
The role requires a Bachelor's degree and 4–7 years of experience, strong written and spoken English, and the ability to navigate guidance documents, prepare amendments, and present findings to
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Level
ManagerL7
Location
Washington, DC
Occupation
Regulatory Affairs Managers
Industry
Electromedical and Electrotherapeutic Apparatus Manufacturing
Posted
yesterday
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