{"schemaVersion":"jobsearcher.job.v1","id":"c88786f5d8aeb47208fe7a56","url":"https://jobsearcher.com/jobs/c88786f5d8aeb47208fe7a56","canonicalUrl":"https://jobsearcher.com/jobs/c88786f5d8aeb47208fe7a56","title":"SR. QUALITY ENGINEER","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 114,000 colleagues serve people in more than 160 countries.\nWORKING AT ABBOTT\nAt Abbott, you can do work that matters, grow, and learn, care for yourself and 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 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 around the world 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 a best place to work for diversity, working mothers, female executives, and scientists.\nTHE OPPORTUNITY\n\nTHE SR, QUALITY ENGINEER POSITION WORKS ONSITE OF OUR TEMECULA, CA LOCATION IN THE ABBOTT VASCULAR DIVISION. Abbott Vascular provides innovative, minimally invasive, and cost-effective products for treatment of vascular disease.\nAbbott Vascular provides innovative, minimally invasive, and cost-effective products for treatment of vascular disease.\nLead on-time completion of Design Control Deliverables\nCreate and ensure on-time execution of Quality Plans for internal development, OEM-based, Clinical Product Development (CPDP), and design change projects\nAccountable for Design Verification and Validation planning & execution, including active cross-functional root-cause analysis investigation & resolution activities\nLead Risk Management activities from product Concept through Commercialization\nLead design test and inspection method development, and lead method validation activities\nEnsure DHF content completion, integrity, and regulatory & standards compliance; collaboratively communicating & resolving gaps\nSupport manufacturing process development & qualification for new product commercialization and product changes\nWHAT YOU’LL WORK ON\nSupport/lead and ensure internal & external audit responses\nSupport/lead and ensure on time product re-certifications\nSupport and ensure the establishment of objective, measurable, discrete, and verifiable customer and product requirements\nSupport and ensure objective component specification definitions, supplied component sampling plan development, and vendor qualifications\nAccountable for development, execution and analysis of biocompatibility and sterilization qualifications\nComplete Document Change Request Reviews in a timely and objective manner\nDevelop and lead other team members.\nPerform other duties and responsibilities as assigned by management.\nSupport/lead all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.\nComplies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.\nComplies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.\nREQUIRED QUALIFICATIONS\nBachelors Degree in Engineering or Technical Field\nan equivalent combination of education and work experience\nMinimum 5 years Previous Quality engineering experience and demonstrated use of Quality tools/methodologies. Detailed knowledge of FDA, GMP, and ISO 13485\nSolid communication and interpersonal skills. Project management and leadership skills, including the demonstrated ability to lead multi-departmental project teams and resolve quality-related issues in a timely and effective manner.\nAdvanced computer skills, including statistical/data analysis and report writing skills.\nPREFERRED QUALIFICATIONS\nMasters Degree Preferred\nPrior medical device experience preferred. ASQ CQE certification preferred. Design for\nSix Sigma and Critical to Quality training and experience preferred.\nExperience working in a broader enterprise/cross-division business unit model preferred.\nAbility to work in a highly matrixed and geographically diverse business environment.\nAbility to work within a team and as an individual contributor in a fast-paced, changing\nAbility to travel approximately 10%, including internationally.\nAPPLY NOW\nLEARN MORE ABOUT OUR HEALTH AND WELLNESS BENEFITS, WHICH PROVIDE THE SECURITY TO HELP YOU AND YOUR FAMILY LIVE FULL LIVES: www.abbottbenefits.com\nFollow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.\nConnect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews.\n\nThe base pay for this position is $75,300.00 – $150,700.00. In specific locations, the pay range may vary from the range posted.","company":"Abbott","rawCompany":"abbott","city":"Temecula","state":"CA","isRemote":false,"isActive":false,"createdAt":"2026-04-12T21:26:12.727Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"},{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"}],"industries":[{"code":"339112","title":"Surgical and Medical Instrument Manufacturing","slug":"surgical-and-medical-instrument-manufacturing"},{"code":"339113","title":"Surgical Appliance and Supplies Manufacturing","slug":"surgical-appliance-and-supplies-manufacturing"},{"code":"334510","title":"Electromedical and Electrotherapeutic Apparatus Manufacturing","slug":"electromedical-and-electrotherapeutic-apparatus-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"SR. QUALITY ENGINEER","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 114,000 colleagues serve people in more than 160 countries.\nWORKING AT ABBOTT\nAt Abbott, you can do work that matters, grow, and learn, care for yourself and 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 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 around the world 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 a best place to work for diversity, working mothers, female executives, and scientists.\nTHE OPPORTUNITY\n\nTHE SR, QUALITY ENGINEER POSITION WORKS ONSITE OF OUR TEMECULA, CA LOCATION IN THE ABBOTT VASCULAR DIVISION. Abbott Vascular provides innovative, minimally invasive, and cost-effective products for treatment of vascular disease.\nAbbott Vascular provides innovative, minimally invasive, and cost-effective products for treatment of vascular disease.\nLead on-time completion of Design Control Deliverables\nCreate and ensure on-time execution of Quality Plans for internal development, OEM-based, Clinical Product Development (CPDP), and design change projects\nAccountable for Design Verification and Validation planning & execution, including active cross-functional root-cause analysis investigation & resolution activities\nLead Risk Management activities from product Concept through Commercialization\nLead design test and inspection method development, and lead method validation activities\nEnsure DHF content completion, integrity, and regulatory & standards compliance; collaboratively communicating & resolving gaps\nSupport manufacturing process development & qualification for new product commercialization and product changes\nWHAT YOU’LL WORK ON\nSupport/lead and ensure internal & external audit responses\nSupport/lead and ensure on time product re-certifications\nSupport and ensure the establishment of objective, measurable, discrete, and verifiable customer and product requirements\nSupport and ensure objective component specification definitions, supplied component sampling plan development, and vendor qualifications\nAccountable for development, execution and analysis of biocompatibility and sterilization qualifications\nComplete Document Change Request Reviews in a timely and objective manner\nDevelop and lead other team members.\nPerform other duties and responsibilities as assigned by management.\nSupport/lead all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.\nComplies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.\nComplies with U.S. Food and Drug Administration (FDA) regulations, other regulatory requirements, Company policies, operating procedures, processes, and task assignments. Maintains positive and cooperative communications and collaboration with all levels of employees, customers, contractors, and vendors.\nREQUIRED QUALIFICATIONS\nBachelors Degree in Engineering or Technical Field\nan equivalent combination of education and work experience\nMinimum 5 years Previous Quality engineering experience and demonstrated use of Quality tools/methodologies. Detailed knowledge of FDA, GMP, and ISO 13485\nSolid communication and interpersonal skills. Project management and leadership skills, including the demonstrated ability to lead multi-departmental project teams and resolve quality-related issues in a timely and effective manner.\nAdvanced computer skills, including statistical/data analysis and report writing skills.\nPREFERRED QUALIFICATIONS\nMasters Degree Preferred\nPrior medical device experience preferred. ASQ CQE certification preferred. Design for\nSix Sigma and Critical to Quality training and experience preferred.\nExperience working in a broader enterprise/cross-division business unit model preferred.\nAbility to work in a highly matrixed and geographically diverse business environment.\nAbility to work within a team and as an individual contributor in a fast-paced, changing\nAbility to travel approximately 10%, including internationally.\nAPPLY NOW\nLEARN MORE ABOUT OUR HEALTH AND WELLNESS BENEFITS, WHICH PROVIDE THE SECURITY TO HELP YOU AND YOUR FAMILY LIVE FULL LIVES: www.abbottbenefits.com\nFollow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity.\nConnect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews.\n\nThe base pay for this position is $75,300.00 – $150,700.00. In specific locations, the pay range may vary from the range posted.","datePosted":"2026-04-12T21:26:12.727Z","dateModified":"2026-04-12T21:26:12.727Z","hiringOrganization":{"@type":"Organization","name":"Abbott","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Temecula","addressRegion":"CA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"c88786f5d8aeb47208fe7a56"},"url":"https://jobsearcher.com/jobs/c88786f5d8aeb47208fe7a56"}}