Pharma Specification Writer - GMP & Documentation Lead

A leading biopharmaceutical manufacturer in Fishers, IN is seeking an experienced Specification Writer. This position involves developing and maintaining material specifications to ensure regulatory compliance and effectiveness. Candidates should have a degree in supply chain management or a related field, along with 2+ years of relevant experience in a GMP environment. Strong collaboration and organizational skills are essential for working with various teams. This role offers the opportunity to contribute to the quality and efficiency of materials used in drug manufacturing. #J-18808-Ljbffr