{"id":4047583,"url":"https://alion.io/job/abbott-manager-laboratory-supplier-quality","title":"Manager, Laboratory Supplier Quality","company":{"id":2710,"name":"Abbott","domain":"abbott.com","url":"https://alion.io/company/abbott","size_band":"5000+","is_staffing_agency":false,"employer_type":"direct","is_intermediary":false,"listed_via":null,"ats_vendor":"Workday","truth_index":{"grade":"B","score":80,"open_postings":346,"ghost_share":0.003,"stale_share":0.766,"repost_share":0.017,"time_to_fill_p50_days":29,"computed_at":"2026-11-12T10:38:37Z"}},"role":"Industrial Engineering","role_family":"Industrial Engineering","seniority":"staff","employment_type":"full_time","work_mode":"on_site","remote_scope":null,"remote_scope_basis":null,"remote_working_hours":null,"hiring_geo_confidence":"explicit","locations":["Madison, United States"],"countries":["US"],"hiring_countries":[],"hiring_countries_total":0,"salary":{"min":99300,"max":198700,"currency":"USD","period":"year","gross":null,"usd_annual":198700},"salary_estimate":null,"experience_years_min":10,"visa_sponsorship":true,"relocation_package":false,"has_equity":false,"technologies":[{"name":"21 CFR Part 820","optional":false},{"name":"ISO 13485","optional":false}],"status":"live","first_seen_at":"2026-11-10T00:00:00Z","employer_posted_date":"2026-11-10","last_verified_at":"2026-11-12T09:51:40Z","board_verified":true,"closed_at":null,"days_open":2,"trust":{"level":"ok","repost_count":null,"flags":[],"days_open":2},"description":"Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 122,000 colleagues serve people in more than 160 countries.JOB DESCRIPTION:\nWorking at Abbott\nAt Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to:\nCareer development with an international company where you can grow the career you dream of.\nEmployees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.\nAn excellent retirement savings plan with a high employer contribution\nTuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.\nA company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.\nA company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.\nPosition Overview\nThe Manager, Laboratory Supplier Quality is responsible for ensuring the quality and regulatory compliance of suppliers supporting clinical laboratory operations for Abbott Cancer Diagnostics by providing leadership in the design, implementation, and continuous improvement of laboratory supplier management processes across the laboratory enterprise.\nThe Manager, Laboratory Supplier Quality acts as the primary Laboratory Quality representative within the enterprise supplier management program, providing guidance on laboratory supplier requirements, proactively identifying and mitigating supplier-related risks, and influencing supplier quality strategy to support regulatory compliance, inspection readiness, operational continuity, and scalable laboratory operations.\nThis role is based in our Madison, WI office location.\nEssential Duties\nInclude, but are not limited to, the following:\nLead the laboratory supplier quality program across the clinical laboratory enterprise, ensuring compliance with CLIA, CAP, ISO 15189, company policies, and applicable regulatory requirements.\nServe as the primary Laboratory Quality representative within the enterprise supplier management program, providing strategic oversight of supplier qualification, approval, governance, risk management, and quality agreements.\nProvide quality and regulatory oversight of suppliers supporting laboratory operations and lead supplier issue management activities, including investigations, corrective actions, audits, assessments, and supplier-related change evaluations.\nIdentify, assess, and mitigate supplier-related risks impacting quality, patient safety, regulatory compliance, operational continuity, and inspection readiness.\nEstablish and monitor supplier quality metrics, performance indicators, and management review processes while driving standardization, continuous improvement, and long-term supplier performance strategies across laboratory sites.\nServe as a supplier quality subject matter expert and trusted advisor to leadership, supporting regulatory inspections, accreditation activities, enterprise quality initiatives, and the development of a culture of quality, compliance, and continuous improvement.\nUphold company mission and values through accountability, innovation, integrity, quality, and teamwork.\nSupport and comply with the company's Quality Management System policies and procedures.\nMaintain regular and reliable attendance.\nAbility to act with an inclusion mindset and model these behaviors for the organization.\nAbility to work designated schedule.\nAbility to work nights and/or weekends, as needed.\nAbility to work on a mobile device, tablet, or in front of a computer screen and/or perform typing for approximately 90% of a typical working day.\nAbility and means to travel between company locations.\nAbility to travel up to 5% of working time away from work location, which may include overnight and weekend travel.\nMinimum Qualifications\nBachelor's Degree in a scientific field, engineering, quality, regulatory affairs, clinical laboratory science, medical technology, or another discipline related to the essential duties of the position.\n10+ years of experience in supplier quality, quality assurance, regulatory compliance, laboratory operations, or related quality functions within a regulated industry.\n6+ years of experience leading cross-functional teams, enterprise initiatives, quality programs, or complex projects.\nDemonstrated experience developing, implementing, and managing supplier qualification, supplier monitoring, supplier auditing, supplier risk management, and supplier corrective action programs.\nDemonstrated experience developing, implementing, and maintaining Quality Management System procedures and practices.\nStrong knowledge of applicable regulations and standards affecting laboratory operations and healthcare products, including CLIA, CAP, ISO 15189, FDA Quality System Regulations, ISO 13485, and applicable state requirements.\nDemonstrated ability to lead enterprise-wide quality initiatives, influence quality strategy, and guide leadership in compliance and risk-based decision making.\nExceptional written, verbal, and interpersonal communication skills.\nStrong analytical, organizational, project management, and problem-solving skills.\nDemonstrated ability to perform the essential duties of the position with or without accommodation.\nAuthorization to work in the United States without sponsorship.\nPreferred Qualifications\nAdvanced degree or Professional certifications in quality, auditing, or compliance (e.g., ASQ CQE, CQA, CMQ/OE, ISO 15189, ISO 13485, or Lead Auditor certification).\nExperience supporting regulatory inspections and accreditation assessments, including CAP, CLIA, FDA, NYSDOH, ISO 15189, or equivalent regulatory frameworks.\nPrevious people leadership experience, including coaching, performance management, talent development, and succession planning.\nDemonstrated expertise in supplier governance, supplier performance management, quality metrics, risk management, and oversight of critical suppliers and service providers.\nKnowledge of continuous improvement methodologies, including Lean, Six Sigma, or other operational excellence frameworks.\nThe base pay for this position is\n$99,300.00 - $198,700.00In specific locations, the pay range may vary from the range posted.\nJOB FAMILY:\nOperations QualityDIVISION:\nONCO Cancer DiagnosticsLOCATION:\nUnited States > Madison : 1 Exact LaneADDITIONAL LOCATIONS:\nWORK SHIFT:\nStandardTRAVEL:\nYes, 5 % of the TimeMEDICAL SURVEILLANCE:\nNoSIGNIFICANT WORK ACTIVITIES:\nContinuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday)Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdfEEO is the Law link - Espanol: 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