{"schemaVersion":"jobsearcher.job.v1","id":"872029df1663d2bb7590ea2b","url":"https://jobsearcher.com/jobs/872029df1663d2bb7590ea2b","canonicalUrl":"https://jobsearcher.com/jobs/872029df1663d2bb7590ea2b","title":"Quality Technician","description":"Job Title: Post Market Quality Technician\nJob Location: Acton, MA\nJob Duration: 03 Months\nShift: Shift Start Time between 6 - 8 am EST\nJob Description:\nThe Post Market Quality Technician plays an integral role in ***'s Quality Department as a hands-on engineering role conducting post market investigations of FDA approved medical devices. The position requires strong organization skills, attention to detail, ability to work in cross functional teams, and drive to accomplish departmental and company goals.\nResponsibilities:\nPerform moderately complex tasks to ensure compliance with quality standards\nPartner with quality assurance engineers and other team members to ensure effective inspection and testing procedures are implemented and maintained\nGenerate, review and maintain Quality records in support of the Quality System, e.g., training, internal audits, Client, and CAPA\nPerform product testing and failure analysis\nReview Lot Acceptance records and DHRs\nCollect log quality data and trend results\nAccountability for quality data entry and productivity\nAssist in gathering information during FDA and ISO 13485 inspections\nTrouble shoot new failure modes.\nEvaluate process and engineering controls to improve safety and efficiency.\nPerform other duties as assigned.\nEducation and Experience:\nMinimum Requirements:\nAssociates Degree in an engineering, or scientific discipline\nPreferred Skills and Competencies:\nElectrical and mechanical background strongly preferred\nPrior experience working in a regulated industry (medical device) and/or experience working in a bio-hazard/lab environment preferred\nPreferred 2 years in a Quality related function, working with QSR and/or ISO 13485\nComputer proficiency in MS office (specifically Excel); experience creating and analyzing charts and Pareto charts a plus\nAbility to organize and complete tasks with minimal supervision\nExcellent technical writing skills\nExcels at generating and maintaining organized and accurate records\nExperience with Lean Six Sigma methodology a plus\nPhysical Requirements (if applicable):\nSitting 70%, Standing 30%\nFrequent lifting","company":"Honorvettechnologies","rawCompany":"honorvettechnologies","city":"Acton","state":"MT","isRemote":false,"isActive":false,"createdAt":"2026-08-13T15:20:49.234Z","occupations":[{"code":"19-4099.01","title":"Quality Control Analysts","slug":"quality-control-analysts"},{"code":"11-3051.01","title":"Quality Control Systems Managers","slug":"quality-control-systems-managers"},{"code":"51-9061.00","title":"Inspectors, Testers, Sorters, Samplers, and Weighers","slug":"inspectors-testers-sorters-samplers-and-weighers"}],"industries":[{"code":"339113","title":"Surgical Appliance and Supplies Manufacturing","slug":"surgical-appliance-and-supplies-manufacturing"},{"code":"334510","title":"Electromedical and Electrotherapeutic Apparatus Manufacturing","slug":"electromedical-and-electrotherapeutic-apparatus-manufacturing"},{"code":"339112","title":"Surgical and Medical Instrument Manufacturing","slug":"surgical-and-medical-instrument-manufacturing"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Quality Technician","description":"Job Title: Post Market Quality Technician\nJob Location: Acton, MA\nJob Duration: 03 Months\nShift: Shift Start Time between 6 - 8 am EST\nJob Description:\nThe Post Market Quality Technician plays an integral role in ***'s Quality Department as a hands-on engineering role conducting post market investigations of FDA approved medical devices. The position requires strong organization skills, attention to detail, ability to work in cross functional teams, and drive to accomplish departmental and company goals.\nResponsibilities:\nPerform moderately complex tasks to ensure compliance with quality standards\nPartner with quality assurance engineers and other team members to ensure effective inspection and testing procedures are implemented and maintained\nGenerate, review and maintain Quality records in support of the Quality System, e.g., training, internal audits, Client, and CAPA\nPerform product testing and failure analysis\nReview Lot Acceptance records and DHRs\nCollect log quality data and trend results\nAccountability for quality data entry and productivity\nAssist in gathering information during FDA and ISO 13485 inspections\nTrouble shoot new failure modes.\nEvaluate process and engineering controls to improve safety and efficiency.\nPerform other duties as assigned.\nEducation and Experience:\nMinimum Requirements:\nAssociates Degree in an engineering, or scientific discipline\nPreferred Skills and Competencies:\nElectrical and mechanical background strongly preferred\nPrior experience working in a regulated industry (medical device) and/or experience working in a bio-hazard/lab environment preferred\nPreferred 2 years in a Quality related function, working with QSR and/or ISO 13485\nComputer proficiency in MS office (specifically Excel); experience creating and analyzing charts and Pareto charts a plus\nAbility to organize and complete tasks with minimal supervision\nExcellent technical writing skills\nExcels at generating and maintaining organized and accurate records\nExperience with Lean Six Sigma methodology a plus\nPhysical Requirements (if applicable):\nSitting 70%, Standing 30%\nFrequent lifting","datePosted":"2026-08-13T15:20:49.234Z","dateModified":"2026-08-13T15:20:49.234Z","hiringOrganization":{"@type":"Organization","name":"Honorvettechnologies","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Acton","addressRegion":"MT","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"872029df1663d2bb7590ea2b"},"url":"https://jobsearcher.com/jobs/872029df1663d2bb7590ea2b"}}