Medical Device Post Market QC Associate

Our client is looking for a Medical Device Post Market QC Associate to support medical device investigations. In this role, you will use your prior background in quality compliance to adhere to processing standards as you receive and unpack returned medical devices. Responsibilities include:Operating safely while consistently following laboratory and quality protocolsEntering data related to each return accurately and promptlyChecking information against lot acceptance records and DHRs to support investigationsCreating, maintaining, and reviewing quality records in a manner consistent with the company's quality systemMaintaining audit readinessQualifications:Education: High School Diploma or higher education1+ year of direct experience in receiving, material handling, or inspection roles within a quality-regulated environmentAbility to work in an environment where you alternate between sitting and standingAbility to lift ~5 pounds, and push/pull upto 50 poundsAbility to work onsite for full-time regular hours Monday-Friday Preferences:Experience working in the medical device industry or working in a biohazard/lab roleProficiency with MS office toolsAbility to generate and maintain records that are accurate and organized