{"schemaVersion":"jobsearcher.job.v1","id":"03613f68368e600a040b59c1","url":"https://jobsearcher.com/jobs/03613f68368e600a040b59c1","canonicalUrl":"https://jobsearcher.com/jobs/03613f68368e600a040b59c1","title":"Process Development Engineer III","description":"By living according to a common set of values, we create a culture that unifies, embraces the uniqueness we all bring to the company, and positions Integer for long-term success.\nAt Integer, our values are embedded in everything we do.\n\nCustomer\nWe focus on our customers' success\nInnovation\nWe create better solutions\nCollaboration\nWe create success together\nInclusion\nWe always interact with others respectfully\nCandor\nWe are open and honest with one another\nIntegrity\nWe do the right things and do things right\n\nThe primary purpose of this position is to apply engineering knowledge and technical problem-solving skills to support process development, manufacturing, and product realization activities. This role is responsible for executing engineering assignments of moderate scope and complexity under the guidance of a Project Manager, Senior Engineer, or Engineering Manager, while serving as the primary technical lead for selected projects. The Engineer III ensures that Integer's internal and external customer expectations are met or exceeded through effective engineering practices, quality compliance, and continuous improvement.\n\nYou adhere to Integer's Values and all safety, environmental, security, and quality requirements including, but not limited to, Quality Management Systems (QMS), Safety, Environmental and Security Management Systems, FDA regulations, company policies, operating procedures, and other applicable regulatory requirements.\nYou support process development activities for new product introduction, product transfers, and process improvement initiatives.\nYou execute engineering projects and assignments under the guidance of Project Managers and Senior Engineers while independently managing assigned workstreams and deliverables.\nYou may serve as the primary technical lead for selected projects of limited to moderate complexity.\nYou develop and optimize manufacturing processes to achieve safety, quality, delivery, and cost objectives.\nYou participate in process characterization activities and utilize data-driven methods to establish robust manufacturing processes.\nYou support and execute process validation activities including Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), and Test Method Validation (TMV).\nYou develop, review, and maintain technical documentation including protocols, reports, work instructions, specifications, engineering studies, and validation documents.\nYou investigate manufacturing issues, perform root cause analysis, and implement corrective and preventive actions.\nYou collaborate with cross-functional teams including Quality, Manufacturing, Operations, Supply Chain, R&D, and Regulatory Affairs to achieve project objectives.\nYou support equipment selection, qualification, and implementation activities as required.\nYou develop and maintain effective working relationships with internal and external stakeholders.\nYou contribute to continuous improvement initiatives that improve product quality, process capability, productivity, and operational efficiency.\nYou perform other duties as assigned by management.\nTechnical Competencies\n\nThe Engineer III is expected to possess working knowledge and hands-on experience in one or more of the following manufacturing and process technologies:\nCleanroom assembly of miniature and precision medical device components.\nLaser welding processes.\nResistance welding processes.\nInjection molding processes.\nSilicone molding processes.\nSterile packaging technologies.\nProcess development and process optimization methodologies.\nStatistical analysis and process characterization techniques.\nMedical device Design Control requirements and documentation.\nRisk management principles and Design for Manufacturability (DFM).\nValidation methodologies including IQ, OQ, PQ, and TMV.\n\nProvide Support of Integer's Manufacturing Excellence and Market Focused Innovation Strategies\n\nYou actively support the deployment of systems, tools, and best practices that drive innovation and continuous improvement.\nYou participate in Manufacturing Excellence initiatives based on the Integer Production System.\nYou contribute to workplace organization, visual management, standardized work, and problem-solving activities.\nYou support process optimization and waste reduction initiatives using Lean and Six Sigma principles.\nYou participate in cross-functional efforts to improve safety, quality, delivery, and cost performance.\nYou contribute ideas and solutions that improve manufacturing capability, process robustness, and customer satisfaction.\n\nHow you will be measured\n\nThe specific measures listed below may be subject to change and are not intended to be an all-inclusive list.\nSafety performance and active participation in Environmental Health & Safety programs.\nAchievement of project objectives, milestones, and deliverables.\nQuality performance and adherence to applicable QMS and regulatory requirements.\nSuccessful execution of process development, characterization, and validation activities.\nTimely completion and quality of engineering documentation.\nProcess improvements resulting in enhanced quality, efficiency, capacity, or cost savings.\nEffective collaboration with cross-functional teams and internal customers.\nContributions to innovation, continuous improvement, and operational excellence initiatives.\nWhat sets you apart\n\nBachelor's Degree in Engineering or a related technical discipline is required.\nTypically, 5-8 years of engineering experience in medical device manufacturing, process development, manufacturing engineering, or a related technical field.\nWorking knowledge of medical device manufacturing processes, particularly cleanroom assembly and related technologies.\nExperience with one or more of the following: laser welding, resistance welding, injection molding, silicone molding, or sterile packaging.\nUnderstanding of Design Controls and medical device product development processes.\nExperience executing process characterization studies and validation activities including IQ, OQ, PQ, and/or TMV.\nFamiliarity with statistical analysis and problem-solving methodologies such as Six Sigma, Root Cause Analysis, 5-Why, and Fishbone Analysis.\nDemonstrated ability to solve technical problems using structured engineering approaches.\nStrong organizational skills with the ability to manage multiple priorities.\nEffective written and verbal communication skills.\nAbility to work independently while collaborating effectively within cross-functional teams.\nPositive attitude, strong work ethic, and commitment to delivering results in a fast-paced manufacturing environment.\nSalary: 96,000-141,000\n\nOur total rewards program is designed to attract, retain, and motivate associates to contribute to Integer's success. Our compensation program includes base salary and a cash-based incentive program supporting our pay-for-performance philosophy. We provide a comprehensive benefits package with immediate eligibility including medical, dental, vision, disability, life insurance, and adoption benefits. Parental leave is available after one year. Optional employee-paid programs include supplemental life insurance, critical illness, hospital indemnity and accident insurance. Employees are immediately eligible to participate in the 401(k) plan with company matching contributions. We provide 80 hours (10 days) of company designated holidays per year plus an annual allotment of paid time off.\n\nU.S. Applicants: Equal Opportunity Employer. In addition, veterans and individuals with disabilities are encouraged to apply.","company":"Integer Holdings","rawCompany":"integer holdings","city":"Minneapolis","state":"MN","isRemote":false,"isActive":false,"createdAt":"2026-08-21T03:32:41.472Z","occupations":[{"code":"17-2112.03","title":"Manufacturing Engineers","slug":"manufacturing-engineers"},{"code":"17-2112.00","title":"Industrial Engineers","slug":"industrial-engineers"},{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"}],"industries":[{"code":"333248","title":"All Other Industrial Machinery Manufacturing","slug":"all-other-industrial-machinery-manufacturing"},{"code":"339113","title":"Surgical Appliance and Supplies Manufacturing","slug":"surgical-appliance-and-supplies-manufacturing"},{"code":"339112","title":"Surgical and Medical Instrument Manufacturing","slug":"surgical-and-medical-instrument-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Process Development Engineer III","description":"By living according to a common set of values, we create a culture that unifies, embraces the uniqueness we all bring to the company, and positions Integer for long-term success.\nAt Integer, our values are embedded in everything we do.\n\nCustomer\nWe focus on our customers' success\nInnovation\nWe create better solutions\nCollaboration\nWe create success together\nInclusion\nWe always interact with others respectfully\nCandor\nWe are open and honest with one another\nIntegrity\nWe do the right things and do things right\n\nThe primary purpose of this position is to apply engineering knowledge and technical problem-solving skills to support process development, manufacturing, and product realization activities. This role is responsible for executing engineering assignments of moderate scope and complexity under the guidance of a Project Manager, Senior Engineer, or Engineering Manager, while serving as the primary technical lead for selected projects. The Engineer III ensures that Integer's internal and external customer expectations are met or exceeded through effective engineering practices, quality compliance, and continuous improvement.\n\nYou adhere to Integer's Values and all safety, environmental, security, and quality requirements including, but not limited to, Quality Management Systems (QMS), Safety, Environmental and Security Management Systems, FDA regulations, company policies, operating procedures, and other applicable regulatory requirements.\nYou support process development activities for new product introduction, product transfers, and process improvement initiatives.\nYou execute engineering projects and assignments under the guidance of Project Managers and Senior Engineers while independently managing assigned workstreams and deliverables.\nYou may serve as the primary technical lead for selected projects of limited to moderate complexity.\nYou develop and optimize manufacturing processes to achieve safety, quality, delivery, and cost objectives.\nYou participate in process characterization activities and utilize data-driven methods to establish robust manufacturing processes.\nYou support and execute process validation activities including Installation Qualification (IQ), Operational Qualification (OQ), Performance Qualification (PQ), and Test Method Validation (TMV).\nYou develop, review, and maintain technical documentation including protocols, reports, work instructions, specifications, engineering studies, and validation documents.\nYou investigate manufacturing issues, perform root cause analysis, and implement corrective and preventive actions.\nYou collaborate with cross-functional teams including Quality, Manufacturing, Operations, Supply Chain, R&D, and Regulatory Affairs to achieve project objectives.\nYou support equipment selection, qualification, and implementation activities as required.\nYou develop and maintain effective working relationships with internal and external stakeholders.\nYou contribute to continuous improvement initiatives that improve product quality, process capability, productivity, and operational efficiency.\nYou perform other duties as assigned by management.\nTechnical Competencies\n\nThe Engineer III is expected to possess working knowledge and hands-on experience in one or more of the following manufacturing and process technologies:\nCleanroom assembly of miniature and precision medical device components.\nLaser welding processes.\nResistance welding processes.\nInjection molding processes.\nSilicone molding processes.\nSterile packaging technologies.\nProcess development and process optimization methodologies.\nStatistical analysis and process characterization techniques.\nMedical device Design Control requirements and documentation.\nRisk management principles and Design for Manufacturability (DFM).\nValidation methodologies including IQ, OQ, PQ, and TMV.\n\nProvide Support of Integer's Manufacturing Excellence and Market Focused Innovation Strategies\n\nYou actively support the deployment of systems, tools, and best practices that drive innovation and continuous improvement.\nYou participate in Manufacturing Excellence initiatives based on the Integer Production System.\nYou contribute to workplace organization, visual management, standardized work, and problem-solving activities.\nYou support process optimization and waste reduction initiatives using Lean and Six Sigma principles.\nYou participate in cross-functional efforts to improve safety, quality, delivery, and cost performance.\nYou contribute ideas and solutions that improve manufacturing capability, process robustness, and customer satisfaction.\n\nHow you will be measured\n\nThe specific measures listed below may be subject to change and are not intended to be an all-inclusive list.\nSafety performance and active participation in Environmental Health & Safety programs.\nAchievement of project objectives, milestones, and deliverables.\nQuality performance and adherence to applicable QMS and regulatory requirements.\nSuccessful execution of process development, characterization, and validation activities.\nTimely completion and quality of engineering documentation.\nProcess improvements resulting in enhanced quality, efficiency, capacity, or cost savings.\nEffective collaboration with cross-functional teams and internal customers.\nContributions to innovation, continuous improvement, and operational excellence initiatives.\nWhat sets you apart\n\nBachelor's Degree in Engineering or a related technical discipline is required.\nTypically, 5-8 years of engineering experience in medical device manufacturing, process development, manufacturing engineering, or a related technical field.\nWorking knowledge of medical device manufacturing processes, particularly cleanroom assembly and related technologies.\nExperience with one or more of the following: laser welding, resistance welding, injection molding, silicone molding, or sterile packaging.\nUnderstanding of Design Controls and medical device product development processes.\nExperience executing process characterization studies and validation activities including IQ, OQ, PQ, and/or TMV.\nFamiliarity with statistical analysis and problem-solving methodologies such as Six Sigma, Root Cause Analysis, 5-Why, and Fishbone Analysis.\nDemonstrated ability to solve technical problems using structured engineering approaches.\nStrong organizational skills with the ability to manage multiple priorities.\nEffective written and verbal communication skills.\nAbility to work independently while collaborating effectively within cross-functional teams.\nPositive attitude, strong work ethic, and commitment to delivering results in a fast-paced manufacturing environment.\nSalary: 96,000-141,000\n\nOur total rewards program is designed to attract, retain, and motivate associates to contribute to Integer's success. Our compensation program includes base salary and a cash-based incentive program supporting our pay-for-performance philosophy. We provide a comprehensive benefits package with immediate eligibility including medical, dental, vision, disability, life insurance, and adoption benefits. Parental leave is available after one year. Optional employee-paid programs include supplemental life insurance, critical illness, hospital indemnity and accident insurance. Employees are immediately eligible to participate in the 401(k) plan with company matching contributions. We provide 80 hours (10 days) of company designated holidays per year plus an annual allotment of paid time off.\n\nU.S. Applicants: Equal Opportunity Employer. In addition, veterans and individuals with disabilities are encouraged to apply.","datePosted":"2026-08-21T03:32:41.472Z","dateModified":"2026-08-21T03:32:41.472Z","hiringOrganization":{"@type":"Organization","name":"Integer Holdings","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Minneapolis","addressRegion":"MN","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"03613f68368e600a040b59c1"},"url":"https://jobsearcher.com/jobs/03613f68368e600a040b59c1"}}