Quality Assurance Specialist

Seeking a quality professional with 4+ years of GMP experience in the pharmaceutical/biopharmaceutical industry to support quality oversight of external manufacturing and testing activities for clinical-stage products. Responsibilities include reviewing batch records, analytical testing documentation, regulatory submissions, source data verification, and supporting batch disposition and quality systems compliance. The role requires strong knowledge of GxP documentation, regulatory requirements, quality systems, and cross-functional collaboration, along with excellent communication and organizational skills. A bachelor's degree in a scientific discipline and proficiency with quality systems and Microsoft Office applications are preferred. #J-18808-Ljbffr