This is an induvidual contributor role.
Small company experience is ideal.
Experience negotiating / communicating with FDA
Experience with submitting regulatory dossiers for reformulations of a currently approved product: includes information on: administrative information, quality, safety, and efficacy.
This role is Hybrid in New Jersy in Somerset county (No remote candidates will be considered) Minimum 1-3 days onsite per week.
Opportunity for contract to hire

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