A leading global biopharmaceutical company is seeking a Quality Documents Expert in Morristown, NJ. This role supports pharmacovigilance and quality operations documentation. Candidates should have a Bachelors degree and at least 2 years of experience in GxP quality systems and pharmacovigilance. Responsibilities include maintaining quality documents, promoting standardization, and delivering relevant training. This position offers excellent health benefits and opportunities for international growth.
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