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Manufacturing Engineer

  • ... Posted on: Feb 18, 2026
  • ... Brooksource
  • ... St Paul, Nebraska
  • ... Salary: Not Available
  • ... Full-time

Manufacturing Engineer   

Job Title :

Manufacturing Engineer

Job Type :

Full-time

Job Location :

St Paul Nebraska United States

Remote :

No

Jobcon Logo Job Description :

Manufacturing EngineerLogistics: Location: Arden Hills, MNDuration: 12+ Month Contract-to-hireStart Date: ASAPOnsite Monday-FridayCitizenship: USC or Green Card RequiredOverviewWe are seeking a Manufacturing Engineer to join a high-volume team responsible for producing lithium batteries used in pacemakers and defibrillators—two of the company’s highest-value product lines. This is a critical backfill role with significant visibility and impact on quality, cost, and operational excellence.The ideal candidate will prioritize precision and quality over speed, ensuring processes are executed correctly and thoroughly in a highly regulated medical device environment.Business ObjectiveThis team designs and manufactures lithium batteries and the fixtures that secure them within pacemakers and defibrillators. These product lines represent two of the largest value streams within the organization. The Manufacturing Engineer will play a key role in supporting validation efforts, new production line setup, and continuous process improvements.Key ResponsibilitiesLead and execute validation activities including IQ, OQ, PQ, and process validationsDevelop and execute validation protocols and scriptsSupport the design and setup of new production linesCollaborate with engineering and operations teams to ensure manufacturing readinessIdentify process gaps, troubleshoot issues, and implement sustainable solutionsEnsure strict adherence to quality standards and regulatory requirementsProactively communicate project status, risks, and roadblocksMaintain strong attention to detail to minimize scrap and prevent quality issuesRequired Qualifications5+ years of manufacturing engineering experience, preferably in medical device or regulated industriesStrong experience with IQ/OQ/PQ and process validationExperience setting up new production linesBackground in mechanical engineering preferred (vs. chemical/electrical focus)Understanding of automation systemsAbility to work independently and manage workload effectivelyStrong communication skills and proactive problem-solving approachHigh attention to detail and commitment to qualityNice to Have:AutoCADSolidWorks

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Jobcon Logo Position Details

Posted:

Feb 18, 2026

Employment:

Full-time

Salary:

Not Available

City:

St Paul

Job Origin:

APPCAST_CPC

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Manufacturing EngineerLogistics: Location: Arden Hills, MNDuration: 12+ Month Contract-to-hireStart Date: ASAPOnsite Monday-FridayCitizenship: USC or Green Card RequiredOverviewWe are seeking a Manufacturing Engineer to join a high-volume team responsible for producing lithium batteries used in pacemakers and defibrillators—two of the company’s highest-value product lines. This is a critical backfill role with significant visibility and impact on quality, cost, and operational excellence.The ideal candidate will prioritize precision and quality over speed, ensuring processes are executed correctly and thoroughly in a highly regulated medical device environment.Business ObjectiveThis team designs and manufactures lithium batteries and the fixtures that secure them within pacemakers and defibrillators. These product lines represent two of the largest value streams within the organization. The Manufacturing Engineer will play a key role in supporting validation efforts, new production line setup, and continuous process improvements.Key ResponsibilitiesLead and execute validation activities including IQ, OQ, PQ, and process validationsDevelop and execute validation protocols and scriptsSupport the design and setup of new production linesCollaborate with engineering and operations teams to ensure manufacturing readinessIdentify process gaps, troubleshoot issues, and implement sustainable solutionsEnsure strict adherence to quality standards and regulatory requirementsProactively communicate project status, risks, and roadblocksMaintain strong attention to detail to minimize scrap and prevent quality issuesRequired Qualifications5+ years of manufacturing engineering experience, preferably in medical device or regulated industriesStrong experience with IQ/OQ/PQ and process validationExperience setting up new production linesBackground in mechanical engineering preferred (vs. chemical/electrical focus)Understanding of automation systemsAbility to work independently and manage workload effectivelyStrong communication skills and proactive problem-solving approachHigh attention to detail and commitment to qualityNice to Have:AutoCADSolidWorks

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