Responsibilities---

Perform incoming inspection per inspection plan requirementsPerform the acceptance of finished devices as the final quality releasePrioritize multiple product lines of varying speeds and volumes to ensure a steady flow of released material.Maintain compliance in a highly regulated environment for Class III medical devices following good documentation practices (GDP)Perform other related duties as assigned.Additional Duties & ResponsibilitiesIdentify, tag, and physically segregate non-conforming materialCreate non-conformance records (NCs) for rejected materialCross functional collaboration, including but not limited to, Manufacturing, Procurement, Distribution, Engineering, Quality, and Regulatory Affairs to ensure coordination of activities