Lead GMP Equipment Validation Specialist

A leading CRO company in New Hampshire is seeking an Equipment Validation Specialist to ensure that critical GMP equipment is validated and compliant with user requirements. Responsibilities include performing validation activities, maintaining validation equipment, and developing protocols. The ideal candidate has a preferred 4-year degree and at least 4 years of manufacturing experience, especially in biopharmaceutical settings. This role is pivotal for ensuring a quality, compliant manufacturing environment.
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