Title: Boston, MA Onsite Required experience & Experience: Typically requires >5 years of relevant industry experience such as materials management, supply chain, quality assurance and/or manufacturing in biotechnology/regulated pharmaceutical environment. This candidate must be a SME in "RAW MATERIALS & cGMP Documentation Vendor Quality Management Specialist * Oversee Raw Material Inventory Management, Segregation, Storage, and Cycle Count. * Responsible for review and approve raw material rec