The primary purpose of the position is inspecting materials and products, and following documented ISO processes and procedures for meeting customer specific requirements. To comply with all necessary regulatory, quality system and business requirements as based on ISO 13485 and FDA requirements for medical device and Food manufacturing. Reporting to the site Quality Manager, the person will need to work closely with the Account Teams, Quality Engineers, Materials Department and any other groups as necessary.This is a 1st shift position: M-F, 6:00 A.M. to 2:00 P.M., overtime may be required.Responsibilities:Inspect product for defects, damage, and imperfectionsBe assertive when a quality issue arisesGather data to resolve quality-related issuesWork with supervision and the account teams to resolve quality issuesFollow all documented processes and proceduresMaintain accurate and thorough record keepingEnsure quality requirements meet or exceed customer requirementsAssist in continuous improvementCross-train in any departmental quality areas as neededComply with all facility safety and work rules; including, but not limited to security requirements, proper procedures for accident/incident reporting, emergency evacuation, etc.Represent RR Donnelley Supply Chain & Packaging Solutions in a professional mannerBe able to lift up to 50 pounds at times, twist/ bend, stand for the whole shift.Duties which may be performed as need arises include:Special projects as assignedPerform and maintain departmental 5S proceduresFollow ISO procedures, participate in ISO audits and trainingWork in other departments as deemed necessary to meet business needs
