Pharma QA Associate — Quality & cGMP Compliance

A growing pharmaceutical company in Fairfield, NJ is seeking a detail-oriented QA Associate to support daily Quality Assurance operations. The ideal candidate should have at least 1 year of experience in a regulated cGMP environment, strong documentation skills, and the ability to multitask. Responsibilities include managing batch records, preparing documentation, and supporting audits. Join a collaborative team committed to quality and continuous improvement. #J-18808-Ljbffr