{"schemaVersion":"jobsearcher.job.v1","id":"bc9feccf0f6c8d270f453413","url":"https://jobsearcher.com/jobs/bc9feccf0f6c8d270f453413","canonicalUrl":"https://jobsearcher.com/jobs/bc9feccf0f6c8d270f453413","title":"Supervisor, Process Engineering","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 115,000 colleagues serve people in more than 160 countries.\nSupervisor, Process Engineering\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.\nThe Opportunity\nAbbott Rapid Diagnostics is part of Abbott’s Diagnostics family of businesses, bringing together exceptional teams of experts and industry leading technologies to support diagnostic testing which provides important information for treatment and management of diseases and other conditions.\nThe Supervisor, Process Engineering position is within our Infectious Disease Business Unit located in Scarborough, Maine. In this role, you will provide tactical leadership within the Engineering organization, ensuring engineering readiness to support manufacturing operations, production objectives, and product transfer activities. You will lead a team of engineers responsible for driving process improvements, supporting new product and equipment initiatives, and advancing operational excellence across the manufacturing environment.\nAs a key member of the organization, you will partner with cross-functional teams to ensure reliable, efficient, and compliant manufacturing processes while representing Engineering in internal and external business meetings. You will also play an important role in maintaining compliance within the company's Quality Management System and supporting continuous improvement initiatives that enhance quality, productivity, and operational performance. Through strong technical leadership, team development, and stakeholder engagement, you will help drive engineering excellence, process capability, and long-term business success.\nWhat You’ll Work On\nLead engineering activities related to process validation, equipment qualification, new product introduction, and manufacturing process development.\nDrive the design, development, and implementation of new manufacturing processes and equipment to support business growth and product portfolio expansion.\nPartner cross-functionally to improve manufacturing performance through scrap reduction, process optimization, and capability improvements.\nProvide technical leadership in resolving production equipment issues and leading root cause investigations for process and product-related failures.\nSupport and lead Corrective and Preventive Actions (CAPA), continuous improvement initiatives, and equipment reliability programs.\nChampion Lean Six Sigma methodologies, including DMAIC and DMADV, to improve operational performance and drive sustainable results.\nDevelop and implement Statistical Process Control (SPC) programs to monitor process performance, reduce variation, and improve yield.\nPromote best practices in manufacturing engineering, controls engineering, equipment design, maintenance, and operational excellence.\nSupport proactive programs focused on Total Productive Maintenance (TPM), equipment reliability, facility contingency planning, machine safety, and emergency response preparedness.\nEnsure compliance with FDA regulations, ISO requirements, Abbott quality standards, and all applicable policies and procedures.\nCollaborate effectively with manufacturing, quality, maintenance, regulatory, and operations teams to achieve business objectives.\nLead, coach, and develop a team of engineering professionals to support plant goals and strategic initiatives.\nCreate a culture of accountability, engagement, and continuous improvement.\nManage employee performance, development planning, and talent growth activities.\nParticipate in recruiting, interviewing, hiring, onboarding, and training team members.\nPrioritize and assign engineering resources to support manufacturing, validation, and capital project activities.\nFoster strong partnerships across departments while driving execution of engineering objectives and operational priorities.\nImprove manufacturing efficiency, process capability, and equipment reliability.\nDrive successful implementation of new technologies, processes, and capital projects.\nStrengthen quality, compliance, and safety performance across operations.\nDevelop high-performing engineering talent while supporting Abbott's commitment to innovation and continuous improvement.\nRequired Qualifications\nBachelor's degree (BS) in Engineering or equivalent combination of education and experience. \n3+ years’ experience in Manufacturing Engineering or Design Engineering \n2+ years’ direct experience in providing engineering support to production. \nPrior experience managing equipment design and development as it relates to high-speed manufacturing processes, automation, fixtures, set-up reduction.\nPREFERRED QUALIFICATIONS:\nPrior experience working in a company operating under ISO, FDA, or similar quality systems or regulations. \nExperience in the application of lean six sigma principles and the DMAIC approach or a similar structured problem-solving system. \nExperience with a mix of in-house development and contract management. \nDemonstrated knowledge of cGMP's and FDA regulations as pertains to process engineering.\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 $78,000.00 – $156,000.00. In specific locations, the pay range may vary from the range posted.","company":"Abbot","rawCompany":"abbot","city":"Briarcliff Manor","state":"NY","isRemote":false,"isActive":false,"createdAt":"2026-08-08T13:29:10.710Z","occupations":[{"code":"51-1011.00","title":"First-Line Supervisors of Production and Operating Workers","slug":"first-line-supervisors-of-production-and-operating-workers"},{"code":"11-9041.00","title":"Architectural and Engineering Managers","slug":"architectural-and-engineering-managers"},{"code":"17-2112.03","title":"Manufacturing Engineers","slug":"manufacturing-engineers"}],"industries":[{"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"},{"code":"339112","title":"Surgical and Medical Instrument Manufacturing","slug":"surgical-and-medical-instrument-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Supervisor, Process Engineering","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 115,000 colleagues serve people in more than 160 countries.\nSupervisor, Process Engineering\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.\nThe Opportunity\nAbbott Rapid Diagnostics is part of Abbott’s Diagnostics family of businesses, bringing together exceptional teams of experts and industry leading technologies to support diagnostic testing which provides important information for treatment and management of diseases and other conditions.\nThe Supervisor, Process Engineering position is within our Infectious Disease Business Unit located in Scarborough, Maine. In this role, you will provide tactical leadership within the Engineering organization, ensuring engineering readiness to support manufacturing operations, production objectives, and product transfer activities. You will lead a team of engineers responsible for driving process improvements, supporting new product and equipment initiatives, and advancing operational excellence across the manufacturing environment.\nAs a key member of the organization, you will partner with cross-functional teams to ensure reliable, efficient, and compliant manufacturing processes while representing Engineering in internal and external business meetings. You will also play an important role in maintaining compliance within the company's Quality Management System and supporting continuous improvement initiatives that enhance quality, productivity, and operational performance. Through strong technical leadership, team development, and stakeholder engagement, you will help drive engineering excellence, process capability, and long-term business success.\nWhat You’ll Work On\nLead engineering activities related to process validation, equipment qualification, new product introduction, and manufacturing process development.\nDrive the design, development, and implementation of new manufacturing processes and equipment to support business growth and product portfolio expansion.\nPartner cross-functionally to improve manufacturing performance through scrap reduction, process optimization, and capability improvements.\nProvide technical leadership in resolving production equipment issues and leading root cause investigations for process and product-related failures.\nSupport and lead Corrective and Preventive Actions (CAPA), continuous improvement initiatives, and equipment reliability programs.\nChampion Lean Six Sigma methodologies, including DMAIC and DMADV, to improve operational performance and drive sustainable results.\nDevelop and implement Statistical Process Control (SPC) programs to monitor process performance, reduce variation, and improve yield.\nPromote best practices in manufacturing engineering, controls engineering, equipment design, maintenance, and operational excellence.\nSupport proactive programs focused on Total Productive Maintenance (TPM), equipment reliability, facility contingency planning, machine safety, and emergency response preparedness.\nEnsure compliance with FDA regulations, ISO requirements, Abbott quality standards, and all applicable policies and procedures.\nCollaborate effectively with manufacturing, quality, maintenance, regulatory, and operations teams to achieve business objectives.\nLead, coach, and develop a team of engineering professionals to support plant goals and strategic initiatives.\nCreate a culture of accountability, engagement, and continuous improvement.\nManage employee performance, development planning, and talent growth activities.\nParticipate in recruiting, interviewing, hiring, onboarding, and training team members.\nPrioritize and assign engineering resources to support manufacturing, validation, and capital project activities.\nFoster strong partnerships across departments while driving execution of engineering objectives and operational priorities.\nImprove manufacturing efficiency, process capability, and equipment reliability.\nDrive successful implementation of new technologies, processes, and capital projects.\nStrengthen quality, compliance, and safety performance across operations.\nDevelop high-performing engineering talent while supporting Abbott's commitment to innovation and continuous improvement.\nRequired Qualifications\nBachelor's degree (BS) in Engineering or equivalent combination of education and experience. \n3+ years’ experience in Manufacturing Engineering or Design Engineering \n2+ years’ direct experience in providing engineering support to production. \nPrior experience managing equipment design and development as it relates to high-speed manufacturing processes, automation, fixtures, set-up reduction.\nPREFERRED QUALIFICATIONS:\nPrior experience working in a company operating under ISO, FDA, or similar quality systems or regulations. \nExperience in the application of lean six sigma principles and the DMAIC approach or a similar structured problem-solving system. \nExperience with a mix of in-house development and contract management. \nDemonstrated knowledge of cGMP's and FDA regulations as pertains to process engineering.\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 $78,000.00 – $156,000.00. In specific locations, the pay range may vary from the range posted.","datePosted":"2026-08-08T13:29:10.710Z","dateModified":"2026-08-08T13:29:10.710Z","hiringOrganization":{"@type":"Organization","name":"Abbot","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Briarcliff Manor","addressRegion":"NY","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"bc9feccf0f6c8d270f453413"},"url":"https://jobsearcher.com/jobs/bc9feccf0f6c8d270f453413"}}