CQV Engineer: End-to-End Equipment Validation in GMP

A pharmaceutical company in South Plainfield is seeking an experienced CQV Engineer to oversee equipment projects from concept to production in a highly regulated environment. The ideal candidate will have over 5 years of CQV experience and a strong hands-on background in equipment validation. Responsibilities include evaluating vendors, leading qualification processes, and ensuring equipment is ready for GMP production. This position involves direct interaction with manufacturing and packaging equipment, making it crucial for candidates to have a technical approach to project ownership.
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