CMC Writer: Regulatory Submissions & Technical Docs

A pharmaceutical recruitment firm is seeking a Pharmaceutical CMC Writer in Paramus, New Jersey. The role involves authoring and reviewing regulatory documents for drug development and ensuring compliance with FDA and EMA guidelines. The ideal candidate will have a degree in chemistry or pharmaceutical sciences and prior experience in regulatory writing. Strong project management and collaboration skills are essential for this position to effectively support high-quality submissions in a timely manner.

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