Senior Method Validation Documentation Lead

Tris Pharma, Inc. in New Jersey is seeking a Method Validation Documentation Specialist to support the MV department. This role requires creating and revising specifications and test methods, as well as preparing annual reports and maintaining SOPs in compliance with regulations. Candidates should hold a Bachelor’s in Chemistry with at least 8 years of experience in analytical development or a Master's with 5 years. The position offers a competitive salary package and additional benefits including bonuses and medical insurance.
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