QA Associate II - GMP Documentation & Batch Release

A biomanufacturing technology firm is seeking an Associate II in Quality Assurance located in Kentucky. This role is essential for overseeing QA activities across various operations including packaging and documentation. Candidates should have experience in the pharmaceutical industry or quality assurance, strong communication skills, and a willingness to learn. The position offers a day shift schedule with a 2/2/3 rotation. An understanding of GMP compliance is crucial for maintaining quality standards. #J-18808-Ljbffr