{"schemaVersion":"jobsearcher.job.v1","id":"2534c3cbeb8dbbbd4cc58d06","url":"https://jobsearcher.com/jobs/2534c3cbeb8dbbbd4cc58d06","canonicalUrl":"https://jobsearcher.com/jobs/2534c3cbeb8dbbbd4cc58d06","title":"Quality Control Technician","description":"Job Title: Quality Technician (Chemistry/Biology)Duration: 12+ Months (Possible extension)Location: Maple Grove, MN 55369Onsite RoleResponsibilities:Chemistry/Biology experience.Operate and maintain test equipment.Will work within a high-performance cross-functional team performing routine medical device particulate testing ensuring delivery of the highest quality result to the customer.Employ basic analytical lab skills such as reading a meniscus, pipetting, using a balance, using a stir plate etc.Performs routine testing assignments requiring basic interpretation of established procedures.Gather and record data, analyze results and verify & report test results.Assignments require broad judgment in troubleshooting.Create and maintain data files and forms.Communicate with a wide variety of personnel in and outside of the plant.Identify areas of improvement and participate in continuous improvement projects.Use documentation systems to research information and generate Change Requests.Assist in developing and qualify data sheets, equipment/fixtures, visual standards, and test methods.Initiate, investigate, and assist in generation and completion of NCEPs and DDAs.Assist with product failure analysis.Communicate testing results to teams.Assist engineers in failure analysis and CAPA activities, including assignment as a CAPA project member.Support process and product qualification activities.Serve support roles during external audits: Document retriever, auditee.Education/Experience:AA Degree or equivalent work experience in related discipline and 3+ year of related experience.Prior experience in a lab environment including analytical laboratory skills (weighing, pipetting, scientific method, etc.).Knowledge of Microsoft Office (Word, Excel, Outlook) is required.Must be physically able to lift up to 35 lbs.Must be able to stand for 8 hours.Preferred:DV test protocol training and execution experiencePrior experience in test documentation through lab notebooks or reports.Experience in medical device industry preferably testing medical devices.Demonstrated experience analyzing and fulfilling documentation requirements.Ability to work in a team environment interacting with engineers and technicians.","company":"Req Solutions","rawCompany":"req solutions","city":"Maple Grove","state":"MN","isRemote":false,"isActive":false,"createdAt":"2026-07-01T10:37:51.899Z","occupations":[{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"},{"code":"19-4031.00","title":"Chemical Technicians","slug":"chemical-technicians"},{"code":"17-3028.00","title":"Calibration Technologists and Technicians","slug":"calibration-technologists-and-technicians"}],"industries":[{"code":"541380","title":"Testing Laboratories and Services","slug":"testing-laboratories-and-services"},{"code":"621511","title":"Medical Laboratories","slug":"medical-laboratories"},{"code":"325413","title":"In-Vitro Diagnostic Substance Manufacturing","slug":"in-vitro-diagnostic-substance-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Quality Control Technician","description":"Job Title: Quality Technician (Chemistry/Biology)Duration: 12+ Months (Possible extension)Location: Maple Grove, MN 55369Onsite RoleResponsibilities:Chemistry/Biology experience.Operate and maintain test equipment.Will work within a high-performance cross-functional team performing routine medical device particulate testing ensuring delivery of the highest quality result to the customer.Employ basic analytical lab skills such as reading a meniscus, pipetting, using a balance, using a stir plate etc.Performs routine testing assignments requiring basic interpretation of established procedures.Gather and record data, analyze results and verify & report test results.Assignments require broad judgment in troubleshooting.Create and maintain data files and forms.Communicate with a wide variety of personnel in and outside of the plant.Identify areas of improvement and participate in continuous improvement projects.Use documentation systems to research information and generate Change Requests.Assist in developing and qualify data sheets, equipment/fixtures, visual standards, and test methods.Initiate, investigate, and assist in generation and completion of NCEPs and DDAs.Assist with product failure analysis.Communicate testing results to teams.Assist engineers in failure analysis and CAPA activities, including assignment as a CAPA project member.Support process and product qualification activities.Serve support roles during external audits: Document retriever, auditee.Education/Experience:AA Degree or equivalent work experience in related discipline and 3+ year of related experience.Prior experience in a lab environment including analytical laboratory skills (weighing, pipetting, scientific method, etc.).Knowledge of Microsoft Office (Word, Excel, Outlook) is required.Must be physically able to lift up to 35 lbs.Must be able to stand for 8 hours.Preferred:DV test protocol training and execution experiencePrior experience in test documentation through lab notebooks or reports.Experience in medical device industry preferably testing medical devices.Demonstrated experience analyzing and fulfilling documentation requirements.Ability to work in a team environment interacting with engineers and technicians.","datePosted":"2026-07-01T10:37:51.899Z","dateModified":"2026-07-01T10:37:51.899Z","hiringOrganization":{"@type":"Organization","name":"Req 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