In this role youAre responsible for performing diverse quality control tasks, supporting the maintenance of drug master production records and the verification system per MPCR. The role assists in implementing quality control procedures and protocols, adhering to Good Laboratory Practices (GLP) and Good Manufacturing Practices (GMP) standards.Your role: * Processing new devices, failed devices and performing QA audits and inspections as required. * Inspection of incoming goods. Perform required testing. Inspection of finished products for final release. * Responsible for performing analysis and documentation of all pending failures from out of box, check-in and field failures and generating summary reports at the service center locations. * Document required information into the quality systems such as NCRs and receiving inspections. * Work closely with Distribution, Braemar, Warehouse and QA personnel on assignments as required.You're the right fit if: * High School Diploma, Vocational Education or equivalent. * Experience in Distribution and inspection * Strong attention to detail, Strong verbal and written communication skills, Solid interpersonal skills, team focused * You must be able to successfully perform the following minimum Physical, Cognitive and Environmental job requirements with or without accommodation for this Office/Remote position. How we work togetherWe believe that we are better together than apart. For our office-based teams, this means working in-person at least 5 days per week. Onsite roles require full-time presence in the company’s facilities. Field roles are most effectively done outside of the company’s main facilities, generally at the customers’ or suppliers’ locations.This is an office role.