{"schemaVersion":"jobsearcher.job.v1","id":"0f317234a4007003b99ba1eb","url":"https://jobsearcher.com/jobs/0f317234a4007003b99ba1eb","canonicalUrl":"https://jobsearcher.com/jobs/0f317234a4007003b99ba1eb","title":"Quality Engineer","description":"Job Title\nQuality Engineer\n\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 a range of benefits, including career development, free medical coverage, a retirement savings plan, tuition reimbursement, and more.\n\nBenefits\n\nCareer development with an international company where you can grow the career of which you dream.\n\nEmployees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.\n\nAn excellent retirement savings plan with high employer contribution.\n\nTuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit – an affordable and convenient path to getting a bachelor’s degree.\n\nA company recognized as a great place to work, named one of the most admired companies by Fortune, and a best place to work for diversity, working mothers, female executives, and scientists.\n\nThe Opportunity\nOur location in Temecula, CA, currently has an opportunity for a Quality Engineer in our Vascular Division. This is a fully onsite role.\n\nThe Quality Engineer assures new or modified products conform to quality standards and establishes compliance with the quality system. Responsible for maintaining a strong collaborative partnership with cross‑functional team members that facilitates organizational success by protecting patient/user safety and meeting business needs.\n\nAbbott Vascular provides innovative, minimally invasive and cost‑effective products for treatment of vascular disease. Our extensive portfolio includes drug‑eluting stents, bare metal stents, guide wires, balloon dilatation catheters, imaging catheters and software, vessel closure devices and peripheral stents.\n\nWhat You’ll Do\n\nExecute and support on‑time completion of Design Control Deliverables.\n\nSupport on‑time execution of Quality Plans for internal development, OEM‑based, Clinical Product Development (CPDP), and design change projects.\n\nAccountable for Design Verification and Validation planning & execution, including active cross‑functional root‑cause analysis investigation & resolution activities.\n\nLead or support Risk Management activities from product Concept through Commercialization.\n\nSupport design test and inspection method development, and lead method validation activities.\n\nEnsure DHF content completion, integrity, and regulatory & standards compliance; collaboratively communicating & resolving gaps.\n\nSupport manufacturing process development & qualification for new product commercialization and product changes.\n\nSupport internal & external audit responses.\n\nSupport product re‑certifications.\n\nSupport the establishment of objective, measurable, discrete, and verifiable customer and product requirements.\n\nSupport objective component specification definitions, supplied component sampling plan development, and vendor qualifications.\n\nSupport execution of biocompatibility and sterilization qualifications.\n\nComplete Document Change Request Reviews in a timely and objective manner.\n\nAdditional duties may be identified by functional management based on the current project/business objectives.\n\nSupport all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.\n\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.\n\nEducation and Experience You’ll Bring\nRequired Experience\n\nBachelor's degree in a related field.\n\n2‑5+ years of related work experience with a basic understanding of the specified functional area, or an equivalent combination of education and work experience.\n\nMedical Devices or other highly regulated industry experience.\n\nUnderstanding of ISO, ASQ, RM/FMEAs and FDA Regulations.\n\nPrevious Quality engineering experience and demonstrated use of Quality tools/methodologies.\n\nAbility to work in a highly matrixed and geographically diverse business environment.\n\nAbility to work within a team and as an individual contributor in a fast‑paced, changing environment.\n\nAbility to leverage and/or engage others to accomplish projects.\n\nStrong verbal and written communications with the ability to effectively communicate at multiple levels in the organization.\n\nMultitasks, prioritizes and meets deadlines in a timely manner.\n\nStrong organizational and follow‑up skills, as well as attention to detail.\n\nAbility to travel approximately 10%, including internationally.\n\nPreferred Experience\n\nExperience working in a broader enterprise/cross‑division business unit model.\n\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\n\nFollow your career aspirations at 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.\n\nConnect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal.\n\nThe base pay for this position is $61,300.00–$122,700.00. In specific locations, the pay range may vary from the range posted.\n\n#J-18808-Ljbffr","company":"SupportFinity","rawCompany":"supportfinity","city":"Temecula","state":"CA","isRemote":false,"isActive":false,"createdAt":"2026-06-18T03:15:05.028Z","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":"Quality Engineer","description":"Job Title\nQuality Engineer\n\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 a range of benefits, including career development, free medical coverage, a retirement savings plan, tuition reimbursement, and more.\n\nBenefits\n\nCareer development with an international company where you can grow the career of which you dream.\n\nEmployees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.\n\nAn excellent retirement savings plan with high employer contribution.\n\nTuition reimbursement, the Freedom 2 Save student debt program and FreeU education benefit – an affordable and convenient path to getting a bachelor’s degree.\n\nA company recognized as a great place to work, named one of the most admired companies by Fortune, and a best place to work for diversity, working mothers, female executives, and scientists.\n\nThe Opportunity\nOur location in Temecula, CA, currently has an opportunity for a Quality Engineer in our Vascular Division. This is a fully onsite role.\n\nThe Quality Engineer assures new or modified products conform to quality standards and establishes compliance with the quality system. Responsible for maintaining a strong collaborative partnership with cross‑functional team members that facilitates organizational success by protecting patient/user safety and meeting business needs.\n\nAbbott Vascular provides innovative, minimally invasive and cost‑effective products for treatment of vascular disease. Our extensive portfolio includes drug‑eluting stents, bare metal stents, guide wires, balloon dilatation catheters, imaging catheters and software, vessel closure devices and peripheral stents.\n\nWhat You’ll Do\n\nExecute and support on‑time completion of Design Control Deliverables.\n\nSupport on‑time execution of Quality Plans for internal development, OEM‑based, Clinical Product Development (CPDP), and design change projects.\n\nAccountable for Design Verification and Validation planning & execution, including active cross‑functional root‑cause analysis investigation & resolution activities.\n\nLead or support Risk Management activities from product Concept through Commercialization.\n\nSupport design test and inspection method development, and lead method validation activities.\n\nEnsure DHF content completion, integrity, and regulatory & standards compliance; collaboratively communicating & resolving gaps.\n\nSupport manufacturing process development & qualification for new product commercialization and product changes.\n\nSupport internal & external audit responses.\n\nSupport product re‑certifications.\n\nSupport the establishment of objective, measurable, discrete, and verifiable customer and product requirements.\n\nSupport objective component specification definitions, supplied component sampling plan development, and vendor qualifications.\n\nSupport execution of biocompatibility and sterilization qualifications.\n\nComplete Document Change Request Reviews in a timely and objective manner.\n\nAdditional duties may be identified by functional management based on the current project/business objectives.\n\nSupport all Company initiatives as identified by management and in support of Quality Management Systems (QMS), Environmental Management Systems (EMS), and other regulatory requirements.\n\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.\n\nEducation and Experience You’ll Bring\nRequired Experience\n\nBachelor's degree in a related field.\n\n2‑5+ years of related work experience with a basic understanding of the specified functional area, or an equivalent combination of education and work experience.\n\nMedical Devices or other highly regulated industry experience.\n\nUnderstanding of ISO, ASQ, RM/FMEAs and FDA Regulations.\n\nPrevious Quality engineering experience and demonstrated use of Quality tools/methodologies.\n\nAbility to work in a highly matrixed and geographically diverse business environment.\n\nAbility to work within a team and as an individual contributor in a fast‑paced, changing environment.\n\nAbility to leverage and/or engage others to accomplish projects.\n\nStrong verbal and written communications with the ability to effectively communicate at multiple levels in the organization.\n\nMultitasks, prioritizes and meets deadlines in a timely manner.\n\nStrong organizational and follow‑up skills, as well as attention to detail.\n\nAbility to travel approximately 10%, including internationally.\n\nPreferred Experience\n\nExperience working in a broader enterprise/cross‑division business unit model.\n\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\n\nFollow your career aspirations at 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.\n\nConnect with us at www.abbott.com, on Facebook at www.facebook.com/Abbott and on Twitter @AbbottNews and @AbbottGlobal.\n\nThe base pay for this position is $61,300.00–$122,700.00. In specific locations, the pay range may vary from the range posted.\n\n#J-18808-Ljbffr","datePosted":"2026-06-18T03:15:05.028Z","dateModified":"2026-06-18T03:15:05.028Z","hiringOrganization":{"@type":"Organization","name":"SupportFinity","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Temecula","addressRegion":"CA","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"0f317234a4007003b99ba1eb"},"url":"https://jobsearcher.com/jobs/0f317234a4007003b99ba1eb"}}