Pharma QA Specialist: GMP & Batch Record Expert

A reputable pharmaceutical company is looking for a QA Associate (IT) located in North Great River, New York. This role involves reviewing batch production records, ensuring they comply with Good Manufacturing Practices and regulatory standards. Candidates should hold a Bachelor’s degree in pharmacy or related fields and have a minimum of 2-3 years of experience in quality assurance within the pharmaceutical sector. Strong attention to detail and familiarity with document management systems are essential, along with the ability to handle multiple batch reviews. The position ensures products are manufactured according to approved processes and specifications. #J-18808-Ljbffr