{"schemaVersion":"jobsearcher.job.v1","id":"a8016ddc0e1788191a3f426c","url":"https://jobsearcher.com/jobs/a8016ddc0e1788191a3f426c","canonicalUrl":"https://jobsearcher.com/jobs/a8016ddc0e1788191a3f426c","title":"Process Engineer","description":"AtriCure, Inc. provides innovative technologies for the treatment of Afib and related conditions. Afib affects more than 33 million people worldwide. Electrophysiologists and cardiothoracic surgeons around the globe use AtriCure technologies for the treatment of Afib and reduction of Afib related complications. AtriCure’s Isolator® Synergy™ Ablation System is the first medical device to receive FDA approval for the treatment of persistent Afib. AtriCure’s AtriClip® Left Atrial Appendage Exclusion System products are the most widely sold LAA management devices worldwide. AtriCure’s Hybrid AF™ Therapy is a minimally invasive procedure that provides a lasting solution for long-standing persistent Afib patients. AtriCure’s cryoICE cryoSPHERE® probe is cleared for temporary ablation of peripheral nerves to block pain, providing pain relief in cardiac and thoracic procedures. For more information, visit AtriCure.com or follow us on Twitter @AtriCure.\r\nWe foster a culture of inclusion by embracing diverse experiences and individuals where everyone’s authentic self is welcome. We offer supporting programs and resources that provide enriching and equitable opportunities for each person to contribute professionally and personally.\r\nPOSITION SUMMARYThe Process Engineer is responsible for on-going production, validations, and continuous improvement of new and existing manufacturing processes. He/she contributes in a creative and collaborative way to achieve the company’s goals of producing market leading products through positive patient outcomes.\r\nESSENTIAL FUNCTIONS OF THE POSITIONTeam member of projects involving design and manufacturing resources, both internal and external. Specific expectations include:\r\nOwnership of product assembly line technical performance. Support production with troubleshooting assembly line issues, resolution of non-conformances, completion of root cause investigations, and CAPA’s\r\nDrive a lean, KPI-driven, and continuous improvement culture across the department\r\nImplement lean principles and methodologies to optimize manufacturing processes.\r\nLead continuous improvement initiatives, including value stream mapping (VSM), 5S and Kaizen events\r\nAnalyze production data to identify bottlenecks, inefficiencies, and opportunities for streamlining\r\nCollaborate with cross-functional engineering team (quality, product development, regulatory) to address product line issues\r\nResponsible for communication of manufacturing and process issues to cross functional engineering team and suppliers, both verbally and in written documentation\r\nReview of proposed component tolerances and input to manufacturing capability\r\nHas knowledge of tolerance capabilities of machining, molding, casting, stamping, forming, grinding, etc.\r\nUnderstands GD&T and how to properly apply it to yield the desired fits between joining parts\r\nReview of proposed device assembly requirements and identification of Design for Assembly opportunities. Understanding of assembly and joining techniques including laser welding, ultrasonic welding, adhesive bonding, over-molding, soldering etc. Understand of error proofing, poke-yoke\r\nWorking knowledge of Manual and Automated Assembly Systems and Technologies\r\nAct as a lean champion to train and mentor others on lean concepts and tools as needed\r\nMANUFACTURING PROCESS KNOWLEDGEKnowledge of general manufacturing technologies (plastic injection molding, stamping, milling, turning, assembly methods, various fastening techniques) including low to medium volume manufacturing processes\r\nFamiliar with manufacturing efficiency strategies such as Lean, Six Sigma, 5S, Value Stream mapping, using SPC in resolving/improving productivity and efficiencies etc.\r\nWork with outside suppliers to define, document, analyze and qualify their manufacturing processes.\r\nIdentify new vendors, processes, materials, and technologies that can be used to improve product quality and reduce product cost\r\nIdentify and implement manufacturing and product-related cost reduction opportunities. Understand life cycle costs and cost benefit analysis. Apply continuous improvement methods to enhance yield, consistency, performance, capacity, etc. of equipment and processes\r\nPerform process capability assessments and establish methods to control process output.\r\nWorking understanding of quality statistical models and metrics (confidence/reliability intervals, DOE, regression/trending, SPC, t-Tests, acceptance plans)\r\nAble to work in a controlled environment where gowning and strict adherence to clean room procedures are required\r\nTOOLING AND EQUIPMENTAble to define, communicate, and develop fixture concepts using internal and external resources. Able to incorporate the capabilities of typical production association into these concepts\r\nWork with designers and engineers in the design and development of manufacturing-related equipment and fixtures\r\nDefine and track project tooling and equipment schedule and cost\r\nResponsible for proper installation of new equipment and setting up proper preventive maintenance and calibration plans\r\nWorking knowledge of Manual and Automated Assembly Systems and Technologies, including both mechanical and control systems\r\nExperienced with mechanical equipment and gauges such as microscopes, soldering stations, ovens/furnaces, UV curing stations, Instron, calipers and other measurement gauges\r\nVERIFICATION AND VALIDATIONResponsible for developing detailed process qualification strategies\r\nAble to define statistical sample sizes as related to variable and attribute data based on established company and industry standards\r\nResponsible for maintaining and updating Process maps and FMEAs\r\nResponsible for writing and executing process qualification protocols and reports\r\nUnderstanding of Test Method Validation, IQ, OQ, PQ approach as defined by AtriCure Quality System\r\nMANUFACTURING LOGISTICSUnderstand supply chains, lead times, and raw material availability\r\nAble to construct Bills of Material, with proper unit of measure and inventory points\r\nWorking knowledge of MRP and other requirement planning systems\r\nAble to conduct time studies and analyze cost variances\r\nTROUBLESHOOTING AND ROOT CAUSE ANALYSISResponsible for evaluating components for conformance to design intent via inspection and functional evaluation\r\nResponsible for trending scrap and failure rates, analyzing failure modes, and developing plans to address root cause issues\r\nResponsible for supporting ongoing manufacturing on a daily basis to allow them to meet required production goals\r\nResponsible for disposition of non-conforming material\r\nDOCUMENTATIONProperly document all work in compliance with AtriCure Quality System requirements\r\nResponsible for process documentation release using tools such as Visio, Excel, Word, Procal and Master Control documentation release systems\r\nWrite detailed, easy to understand process instructions\r\nWrite detailed test protocols and reports to document qualification activities\r\nADDITIONAL ESSENTIAL FUNCTIONS OF THE POSITIONRegular and predictable worksite attendance\r\nAbility to work under fast-paced conditions\r\nAbility to make decisions and use good judgement\r\nAbility to prioritize various duties and multitask as required\r\nAbility to successfully work with others\r\nAdditional duties as assigned\r\nBASIC QUALIFICATIONSBachelor’s degree in engineering (mechanical, industrial, or related field) required or demonstrated equivalent combination of education, training, and experience\r\n3 + years of relevant experience\r\nDemonstrated Mechanical and/or Process Engineering ability\r\nSolid understanding of external standards, design controls, quality controls, manufacturing methods\r\nDemonstrates the ability to plan and track tasks to align with project plan and team objectives\r\nDemonstrates excellent written and oral communication skills\r\nDemonstrates excellent ability to work on and influence cross functional teams\r\nDemonstrated ability with data analysis, problem-solving, and troubleshooting\r\nCapable of prioritizing tasks and provide a timely schedule of completion\r\nAbility to travel 5%\r\nPREFERRED QUALIFICATIONSMedical device industry experience\r\nLean Six Sigma certification (Green Belt (or) Black Belt)\r\nDemonstrated lean manufacturing process implementation experience.\r\nProficiency in lean tools such as 5S, Kanban, VSM etc.\r\nSolid understanding of Industry regulations as it pertains to medical devices\r\nOTHER REQUIREMENTSAbility to regularly walk, sit, or stand as required\r\nAbility to occasionally bend and push/pull\r\nAbility to regularly lift up to 10 pounds, occasionally lift over 50 pounds\r\nAbility to pass pre-employment drug screen and background check\r\nAtriCure has a variety of benefits available for US based employees and their families. Examples include:\r\nMedical & Dental beginning day 1 of employment\r\n401K plus match\r\n30 days of paid Parental Leave, in addition to maternity leave, for new moms and dads\r\nVolunteer Time off\r\nPet Insurance\r\nand more\r\nCorporate-based employees also have full access to our on-site fitness center and cafeteria. To see a complete list of our benefits, please visit our careers website: https://www.atricure.com/careers-atricure/benefits.\r\nAtriCure participates in the federal E-Verify program to confirm the identity of and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here https://www.e-verify.gov AtriCure is an Equal Employment Opportunity/Affirmative Action employer and provides Drug Free Workplaces. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national or ethnic origin, age, protected veteran status, status as an individual with disability, sexual orientation, gender identity or any other characteristic protected by federal, state, or local law(s).\r\nYou may access our global privacy policy here: https://www.atricure.com/privacy#J-18808-Ljbffr","company":"Socketdev","rawCompany":"socketdev","city":"Mason","state":"OH","isRemote":false,"isActive":false,"createdAt":"2026-08-25T04:02:28.979Z","occupations":[{"code":"17-2112.03","title":"Manufacturing Engineers","slug":"manufacturing-engineers"},{"code":"17-2112.00","title":"Industrial Engineers","slug":"industrial-engineers"},{"code":"17-3026.00","title":"Industrial Engineering Technologists and Technicians","slug":"industrial-engineering-technologists-and-technicians"}],"industries":[{"code":"339112","title":"Surgical and Medical Instrument Manufacturing","slug":"surgical-and-medical-instrument-manufacturing"},{"code":"334510","title":"Electromedical and Electrotherapeutic Apparatus Manufacturing","slug":"electromedical-and-electrotherapeutic-apparatus-manufacturing"},{"code":"339113","title":"Surgical Appliance and Supplies Manufacturing","slug":"surgical-appliance-and-supplies-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Process Engineer","description":"AtriCure, Inc. provides innovative technologies for the treatment of Afib and related conditions. Afib affects more than 33 million people worldwide. Electrophysiologists and cardiothoracic surgeons around the globe use AtriCure technologies for the treatment of Afib and reduction of Afib related complications. AtriCure’s Isolator® Synergy™ Ablation System is the first medical device to receive FDA approval for the treatment of persistent Afib. AtriCure’s AtriClip® Left Atrial Appendage Exclusion System products are the most widely sold LAA management devices worldwide. AtriCure’s Hybrid AF™ Therapy is a minimally invasive procedure that provides a lasting solution for long-standing persistent Afib patients. AtriCure’s cryoICE cryoSPHERE® probe is cleared for temporary ablation of peripheral nerves to block pain, providing pain relief in cardiac and thoracic procedures. For more information, visit AtriCure.com or follow us on Twitter @AtriCure.\r\nWe foster a culture of inclusion by embracing diverse experiences and individuals where everyone’s authentic self is welcome. We offer supporting programs and resources that provide enriching and equitable opportunities for each person to contribute professionally and personally.\r\nPOSITION SUMMARYThe Process Engineer is responsible for on-going production, validations, and continuous improvement of new and existing manufacturing processes. He/she contributes in a creative and collaborative way to achieve the company’s goals of producing market leading products through positive patient outcomes.\r\nESSENTIAL FUNCTIONS OF THE POSITIONTeam member of projects involving design and manufacturing resources, both internal and external. Specific expectations include:\r\nOwnership of product assembly line technical performance. Support production with troubleshooting assembly line issues, resolution of non-conformances, completion of root cause investigations, and CAPA’s\r\nDrive a lean, KPI-driven, and continuous improvement culture across the department\r\nImplement lean principles and methodologies to optimize manufacturing processes.\r\nLead continuous improvement initiatives, including value stream mapping (VSM), 5S and Kaizen events\r\nAnalyze production data to identify bottlenecks, inefficiencies, and opportunities for streamlining\r\nCollaborate with cross-functional engineering team (quality, product development, regulatory) to address product line issues\r\nResponsible for communication of manufacturing and process issues to cross functional engineering team and suppliers, both verbally and in written documentation\r\nReview of proposed component tolerances and input to manufacturing capability\r\nHas knowledge of tolerance capabilities of machining, molding, casting, stamping, forming, grinding, etc.\r\nUnderstands GD&T and how to properly apply it to yield the desired fits between joining parts\r\nReview of proposed device assembly requirements and identification of Design for Assembly opportunities. Understanding of assembly and joining techniques including laser welding, ultrasonic welding, adhesive bonding, over-molding, soldering etc. Understand of error proofing, poke-yoke\r\nWorking knowledge of Manual and Automated Assembly Systems and Technologies\r\nAct as a lean champion to train and mentor others on lean concepts and tools as needed\r\nMANUFACTURING PROCESS KNOWLEDGEKnowledge of general manufacturing technologies (plastic injection molding, stamping, milling, turning, assembly methods, various fastening techniques) including low to medium volume manufacturing processes\r\nFamiliar with manufacturing efficiency strategies such as Lean, Six Sigma, 5S, Value Stream mapping, using SPC in resolving/improving productivity and efficiencies etc.\r\nWork with outside suppliers to define, document, analyze and qualify their manufacturing processes.\r\nIdentify new vendors, processes, materials, and technologies that can be used to improve product quality and reduce product cost\r\nIdentify and implement manufacturing and product-related cost reduction opportunities. Understand life cycle costs and cost benefit analysis. Apply continuous improvement methods to enhance yield, consistency, performance, capacity, etc. of equipment and processes\r\nPerform process capability assessments and establish methods to control process output.\r\nWorking understanding of quality statistical models and metrics (confidence/reliability intervals, DOE, regression/trending, SPC, t-Tests, acceptance plans)\r\nAble to work in a controlled environment where gowning and strict adherence to clean room procedures are required\r\nTOOLING AND EQUIPMENTAble to define, communicate, and develop fixture concepts using internal and external resources. Able to incorporate the capabilities of typical production association into these concepts\r\nWork with designers and engineers in the design and development of manufacturing-related equipment and fixtures\r\nDefine and track project tooling and equipment schedule and cost\r\nResponsible for proper installation of new equipment and setting up proper preventive maintenance and calibration plans\r\nWorking knowledge of Manual and Automated Assembly Systems and Technologies, including both mechanical and control systems\r\nExperienced with mechanical equipment and gauges such as microscopes, soldering stations, ovens/furnaces, UV curing stations, Instron, calipers and other measurement gauges\r\nVERIFICATION AND VALIDATIONResponsible for developing detailed process qualification strategies\r\nAble to define statistical sample sizes as related to variable and attribute data based on established company and industry standards\r\nResponsible for maintaining and updating Process maps and FMEAs\r\nResponsible for writing and executing process qualification protocols and reports\r\nUnderstanding of Test Method Validation, IQ, OQ, PQ approach as defined by AtriCure Quality System\r\nMANUFACTURING LOGISTICSUnderstand supply chains, lead times, and raw material availability\r\nAble to construct Bills of Material, with proper unit of measure and inventory points\r\nWorking knowledge of MRP and other requirement planning systems\r\nAble to conduct time studies and analyze cost variances\r\nTROUBLESHOOTING AND ROOT CAUSE ANALYSISResponsible for evaluating components for conformance to design intent via inspection and functional evaluation\r\nResponsible for trending scrap and failure rates, analyzing failure modes, and developing plans to address root cause issues\r\nResponsible for supporting ongoing manufacturing on a daily basis to allow them to meet required production goals\r\nResponsible for disposition of non-conforming material\r\nDOCUMENTATIONProperly document all work in compliance with AtriCure Quality System requirements\r\nResponsible for process documentation release using tools such as Visio, Excel, Word, Procal and Master Control documentation release systems\r\nWrite detailed, easy to understand process instructions\r\nWrite detailed test protocols and reports to document qualification activities\r\nADDITIONAL ESSENTIAL FUNCTIONS OF THE POSITIONRegular and predictable worksite attendance\r\nAbility to work under fast-paced conditions\r\nAbility to make decisions and use good judgement\r\nAbility to prioritize various duties and multitask as required\r\nAbility to successfully work with others\r\nAdditional duties as assigned\r\nBASIC QUALIFICATIONSBachelor’s degree in engineering (mechanical, industrial, or related field) required or demonstrated equivalent combination of education, training, and experience\r\n3 + years of relevant experience\r\nDemonstrated Mechanical and/or Process Engineering ability\r\nSolid understanding of external standards, design controls, quality controls, manufacturing methods\r\nDemonstrates the ability to plan and track tasks to align with project plan and team objectives\r\nDemonstrates excellent written and oral communication skills\r\nDemonstrates excellent ability to work on and influence cross functional teams\r\nDemonstrated ability with data analysis, problem-solving, and troubleshooting\r\nCapable of prioritizing tasks and provide a timely schedule of completion\r\nAbility to travel 5%\r\nPREFERRED QUALIFICATIONSMedical device industry experience\r\nLean Six Sigma certification (Green Belt (or) Black Belt)\r\nDemonstrated lean manufacturing process implementation experience.\r\nProficiency in lean tools such as 5S, Kanban, VSM etc.\r\nSolid understanding of Industry regulations as it pertains to medical devices\r\nOTHER REQUIREMENTSAbility to regularly walk, sit, or stand as required\r\nAbility to occasionally bend and push/pull\r\nAbility to regularly lift up to 10 pounds, occasionally lift over 50 pounds\r\nAbility to pass pre-employment drug screen and background check\r\nAtriCure has a variety of benefits available for US based employees and their families. Examples include:\r\nMedical & Dental beginning day 1 of employment\r\n401K plus match\r\n30 days of paid Parental Leave, in addition to maternity leave, for new moms and dads\r\nVolunteer Time off\r\nPet Insurance\r\nand more\r\nCorporate-based employees also have full access to our on-site fitness center and cafeteria. To see a complete list of our benefits, please visit our careers website: https://www.atricure.com/careers-atricure/benefits.\r\nAtriCure participates in the federal E-Verify program to confirm the identity of and employment authorization of all newly hired employees. For further information about the E-Verify program, please click here https://www.e-verify.gov AtriCure is an Equal Employment Opportunity/Affirmative Action employer and provides Drug Free Workplaces. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national or ethnic origin, age, protected veteran status, status as an individual with disability, sexual orientation, gender identity or any other characteristic protected by federal, state, or local law(s).\r\nYou may access our global privacy policy here: https://www.atricure.com/privacy#J-18808-Ljbffr","datePosted":"2026-08-25T04:02:28.979Z","dateModified":"2026-08-25T04:02:28.979Z","hiringOrganization":{"@type":"Organization","name":"Socketdev","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Mason","addressRegion":"OH","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"a8016ddc0e1788191a3f426c"},"url":"https://jobsearcher.com/jobs/a8016ddc0e1788191a3f426c"}}