{"id":2871602,"url":"https://alion.io/job/getinge-qc-technician-ii-2","title":"QC Technician II","company":{"id":719311,"name":"Getinge","domain":"getinge.com","url":"https://alion.io/company/getinge-2","size_band":"5000+","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"SuccessFactors","truth_index":{"grade":"A","score":100,"open_postings":7,"ghost_share":0,"stale_share":0,"repost_share":0,"time_to_fill_p50_days":24,"computed_at":"2026-10-26T05:57:25Z"}},"role":"Field & Service","role_family":"Field & Service","seniority":"middle","employment_type":null,"work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"structured","locations":["Wayne, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":{"min":27,"max":31,"currency":"USD","period":"hour","gross":null,"usd_annual":62000},"salary_estimate":null,"experience_years_min":3,"visa_sponsorship":false,"relocation_package":false,"has_equity":false,"technologies":[],"status":"live","first_seen_at":"2026-10-19T19:52:34Z","employer_posted_date":"2026-10-19","last_verified_at":"2026-10-26T12:39:37Z","board_verified":true,"closed_at":null,"days_open":6,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":6},"description":"With a passion for life\nJoin our diverse teams of passionate people and a career that allows you to develop both personally and professionally. At Getinge we exist to make life-saving technology accessible for more people. To make a true difference for our customers - and to save more lives, we need team players, forward thinkers, and game changers.\nAre you looking for an inspiring career? You just found it.\nJob Overview\nThe Quality Control Technician II is responsible for the administration and execution of the Nonconforming Material Report (NCMR) process. This position manages the lifecycle of nonconforming material from NCMR creation through final disposition, ensuring compliance with quality system requirements and inventory controls. The role performs SAP transactions to place material on quality hold, maintain inventory segregation, and release material following approved disposition. The position also provides support to Incoming Inspection activities and serves as a backup resource for receiving inspection operations.\nJob Responsibilities and Essential Duties\nCreate, initiate, and maintain Nonconforming Material Reports (NCMRs) in accordance with Quality System procedures.\nReview nonconforming material documentation for accuracy, completeness, and compliance.\nCoordinate NCMR activities between Manufacturing, Quality Engineering, Supplier Quality, Materials, and Operations.\nFacilitate timely review and disposition of nonconforming material by the appropriate stakeholders.\nMaintain NCMR metrics and provide status updates to management.\nEnsure proper documentation of dispositions including: Use-As-Is, Rework, Return to Vendor (RTV), Scrap\nVerify all required approvals and supporting documentation are completed prior to NCMR closure.\nParticipate in Material Review Board (MRB) meetings as required.\nSupport investigations related to nonconforming material.\nMaintain accurate inventory status for restricted, quarantined, and dispositioned materials.\nCoordinate SAP material movements associated with NCMR dispositions.\nInvestigate and resolve inventory discrepancies related to quality holds and released material.\nMinimum Requirements\nA High School diploma, or equivalent, is required; 2 years technical school or equivalent experience preferred.\nMinimum 3 years of experience in quality functions within a regulated environment; FDA-regulated medical device experience ideal. \nRequired Knowledge, Skills and Abilities\nStrong organizational and follow-up skills\nStrong written and verbal communication skills, attention to detail and data accuracy.\nExperience using SAP or other ERP systems required.\nAbility to interpret procedures, specifications, and manufacturing documentation.\nMinimum 2 years of experience in a quality, manufacturing, or regulated industry environment.\nExperience with NCMRs, nonconforming material control, or quality systems preferred.\nMedical device, pharmaceutical, or other regulated industry experience preferred.\nThis role is based in Wayne, NJ. The salary range for this position is $27.00 to $31.00 per hour\nThis role is eligible for participation in our Excellence Incentive Plan (EIP), an annual incentive program that rewards performance against financial and operational goals.\nThis shift reports at Monday - Friday 7:00 am to 3:30 pm EST\n#LI-JF1\nAbout us\nWith a firm belief that every person and community should have access to the best possible care, Getinge provides hospitals and life science institutions with products and solutions aiming to improve clinical results and optimize workflows. The offering includes products and solutions for intensive care, cardiovascular procedures, operating rooms, sterile reprocessing and life science. Getinge employs over 12,000 people worldwide and the products are sold in more than 135 countries.\nBenefits at Getinge:\nAt Getinge, we offer a comprehensive benefits package, which includes:\nHealth, Dental, and Vision insurance benefits\n401k plan with company match\nPaid Time Off\nWellness initiative & Health Assistance Resources\nLife Insurance\nShort and Long Term Disability Benefits\nHealth and Dependent Care Flexible Spending Accounts\nCommuter Benefits\nParental and Caregiver Leave\nTuition Reimbursement\nGetinge is an equal opportunity employer and all qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, pregnancy, genetic information, national origin, disability, protected veteran status or any other characteristic protected by law. 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