GMP Documentation Control Technician

kdc/one Port Jervis seeks a dedicated candidate to maintain pharmaceutical product documentation in compliance with FDA regulations. Responsibilities include reviewing records for regulatory audits, managing OTC product documentation, and ensuring adherence to current good manufacturing practices (cGMP).
Applicants should hold a High School diploma and have at least 1 year of relevant experience. The role demands good organizational skills and the ability to effectively follow instructions.

#J-18808-Ljbffr