{"schemaVersion":"jobsearcher.job.v1","id":"fa1fbfa719e9fb51a0d00d97","url":"https://jobsearcher.com/jobs/fa1fbfa719e9fb51a0d00d97","canonicalUrl":"https://jobsearcher.com/jobs/fa1fbfa719e9fb51a0d00d97","title":"Quality Engineer","description":"Manage Corrective and Preventive Actions (CAPA) process and assist owners with quality issues/nonconformances across all Caerus Corp. business units to execute the CAPA process in a compliant and timely manner.\nSupport CAPA owners through CAPA phases and ensure they follow the CAPA process and deliver solid quality records of their actions.\nWork closely with issue identifiers and owners to assess whether new product or quality system issues will escalate to CAPA investigation.\nPrepare reports and/or necessary documentation (i.e., CAPA) and provide support to applicable stakeholders, both internal and external.\nSupport customer and/or patient complaint investigations and complete required documentation.\nParticipate in audit and inspection preparation, resolution of audit and inspection findings and liaise with auditing groups and inspectors through all stages of the audits.\nWork directly with operating entities to provide process analyses oversight on a continuing basis to enforce requirements and meet regulations.\nAssist in legal requests in support of government investigations or litigations.\nEnsure the quality assurance programs and policies are maintained and modified regularly.\nPerform statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications.\nCollect and analyze process defect data for product/process improvement efforts (e.g. scrap, nonconforming product, customer/patient complaints.\nEvaluate the adequacy and compliance of systems, operations, and practices against regulations and company documentation.\nUtilize quality tools to include Risk analysis FMEA, statistical techniques including six-sigma and DOE (design of experiments), root cause analysis, reading and correcting process documents.\nSupport product/process validation, design change and review, quality planning, and risk evaluation.\nSupport engineering, production, and various business unit projects in document control practices.\nParticipate in Continuous Improvement Projects (CIP) for both process and business systems.\nParticipate in the development of a company-wide safety program.\nParticipate in the development of a company-wide training program of the QMS.\nBachelors degree in Engineering, Science or technical field required.\nMinimum of 3 years of related experience in quality assurance (medical device industry preferred).\nWorking knowledge of Quality System Regulation (QSR 21 CFR 820), and ISO 13485:2016.\nStrong verbal and written communication skills.\nMust be comfortable working in an environment with animals.\nProficient in use of computer systems and software: Microsoft Word and Excel (charts, graphs, macros, logging, tracking/trending data), PowerPoint presentations, Adobe Acrobat.\nNetSuite ERP/MRP experience preferred.\nCompensation and Benefits:\nMedical, dental, vision, basic life, voluntary life and A&D, holiday pay, paid time off, bi-annual performance bonus.\nExempt: $70,000 - $90,000. DOE","company":"Caerus","rawCompany":"caerus","city":"Blaine","state":"MN","isRemote":false,"isActive":false,"createdAt":"2026-04-12T20:42:25.168Z","occupations":[{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"},{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"}],"industries":[{"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"},{"code":"541690","title":"Other Scientific and Technical Consulting Services","slug":"other-scientific-and-technical-consulting-services"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Quality Engineer","description":"Manage Corrective and Preventive Actions (CAPA) process and assist owners with quality issues/nonconformances across all Caerus Corp. business units to execute the CAPA process in a compliant and timely manner.\nSupport CAPA owners through CAPA phases and ensure they follow the CAPA process and deliver solid quality records of their actions.\nWork closely with issue identifiers and owners to assess whether new product or quality system issues will escalate to CAPA investigation.\nPrepare reports and/or necessary documentation (i.e., CAPA) and provide support to applicable stakeholders, both internal and external.\nSupport customer and/or patient complaint investigations and complete required documentation.\nParticipate in audit and inspection preparation, resolution of audit and inspection findings and liaise with auditing groups and inspectors through all stages of the audits.\nWork directly with operating entities to provide process analyses oversight on a continuing basis to enforce requirements and meet regulations.\nAssist in legal requests in support of government investigations or litigations.\nEnsure the quality assurance programs and policies are maintained and modified regularly.\nPerform statistical analysis to assess the cost of and determine the responsibility for products or materials that do not meet required standards and specifications.\nCollect and analyze process defect data for product/process improvement efforts (e.g. scrap, nonconforming product, customer/patient complaints.\nEvaluate the adequacy and compliance of systems, operations, and practices against regulations and company documentation.\nUtilize quality tools to include Risk analysis FMEA, statistical techniques including six-sigma and DOE (design of experiments), root cause analysis, reading and correcting process documents.\nSupport product/process validation, design change and review, quality planning, and risk evaluation.\nSupport engineering, production, and various business unit projects in document control practices.\nParticipate in Continuous Improvement Projects (CIP) for both process and business systems.\nParticipate in the development of a company-wide safety program.\nParticipate in the development of a company-wide training program of the QMS.\nBachelors degree in Engineering, Science or technical field required.\nMinimum of 3 years of related experience in quality assurance (medical device industry preferred).\nWorking knowledge of Quality System Regulation (QSR 21 CFR 820), and ISO 13485:2016.\nStrong verbal and written communication skills.\nMust be comfortable working in an environment with animals.\nProficient in use of computer systems and software: Microsoft Word and Excel (charts, graphs, macros, logging, tracking/trending data), PowerPoint presentations, Adobe Acrobat.\nNetSuite ERP/MRP experience preferred.\nCompensation and Benefits:\nMedical, dental, vision, basic life, voluntary life and A&D, holiday pay, paid time off, bi-annual performance bonus.\nExempt: $70,000 - $90,000. DOE","datePosted":"2026-04-12T20:42:25.168Z","dateModified":"2026-04-12T20:42:25.168Z","hiringOrganization":{"@type":"Organization","name":"Caerus","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Blaine","addressRegion":"MN","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"fa1fbfa719e9fb51a0d00d97"},"url":"https://jobsearcher.com/jobs/fa1fbfa719e9fb51a0d00d97"}}