Senior Method Validation Documentation Specialist

A biopharmaceutical company located in South Brunswick, New Jersey, is seeking a Method Validation Documentation Specialist. This role entails managing specifications and associated documents in compliance with cGMP and company policies. Qualified candidates should have a Bachelor's in Chemistry with at least 8 years of relevant experience, or a Master's with a minimum of 5 years. The position offers a salary range of $80k-$100k along with various benefits including health insurance and a 401K plan.
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