Regulatory Affairs Associate

Integrated Resources, Inc ( IRI )

Rahway, NJ

Job Description:

The specialist position is responsible for maintaining the US pharma products registrations and providing CVM/FDA support for labeling and chemistry, manufacturing, and controls (CMC) submissions. The specialist position also works as part of a team to prepare and submit marketed product reports to the regulatory authorities; maintains US state registrations, labeling, drug... More Detail

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