{"schemaVersion":"jobsearcher.job.v1","id":"2c55731b113e3067390ecfb4","url":"https://jobsearcher.com/jobs/2c55731b113e3067390ecfb4","canonicalUrl":"https://jobsearcher.com/jobs/2c55731b113e3067390ecfb4","title":"Validation Engineer","description":"Defibtech is seeking a Validation Engineer to join our Research & Development team! This position will be based onsite at our Guilford, Connecticut site, with hybrid flexibility. The Validation Engineer will have primary responsibilities in planning, designing, developing, implementing, and monitoring the validation strategies that support the release of next generation medical devices. In this role, you will function as a cross functional team member developing test protocols based on requirements, documentation, and feedback to impact patient outcomes.\nCore Responsibilities: Supports the development of validation plans for medical device design functions (software, electrical and mechanical), defines appropriate test methods and apply statistical methods to identify sample sizes.\nDevelops and executes validation protocols based on system requirements and approved procedures and standards (ISO and FDA).\nCollates, analyzes, summarizes, and interprets validation protocol results into cohesive reporting for FDA and CE Mark approvals.\nProperly documents activities in accordance with best engineering practices, company procedures, and regulatory requirements.\nParticipates in Design Reviews and provides verification support to development teams (e.g., Code Reviews, Software Module and System testing, test automation, testing procedures).\nDesigns test equipment, test fixtures, and testing software for diagnosis of medical devices.\nDemonstrates Defibtech’s values on the job and promotes and participates in continuous improvement.\nActively supports compliance of Company operations to all applicable laws, regulations and standards, good business practices and company documented procedures (including but not limited to FDA, Quality Management Systems Regulations, safety regulations, and applicable statutes).\nQualifications / Requirements: Bachelor’s degree and 0-2 years of related experience or the equivalent combination of education, experience, and training.\nPreferred candidates will have a bachelor’s degree in a science-related field such as an engineering discipline (e.g., electrical engineering, biomedical, mechanical, and/or computer science) and 2+ years of relevant experience.\nPrevious experience in supporting manufacturing of electronic or electromechanical products in medical device industry, highly preferred.\nPrevious experience working with conventional inspection and measurement equipment, preferred.\nKnowledge of design verification and validation process and practices, preferred.\nKnowledge of engineering design, test, and safety standards (IEC 60601-1 4TH Edition, FDA, ISO), preferred.\nStrong analytical and problem-solving ability.\nStrong technical writing ability for design validations and reports.\nStrong written and oral communication skills to accurately convey issues and information.\nStrong organizational skills and attention to detail.\nAbility to support multiple projects concurrently while maintaining quality and meeting deadlines.\nAbility to work independently and with a team.\nWork Environment and Physical Demands: Work environment is primary based in an office and frequently within an engineering lab setting. Hybrid remote capable.\nPhysical demands are primarily light work which includes sitting as well as frequent walking/standing throughout location(s) and lifting up to 20lbs to carry lightweight test equipment, fixtures, and devices.\nCompensation and Benefits: Defibtech offers competitive salaries and a comprehensive benefits package including core health benefits, company-paid disability, and a company matching 401k plan.\nDefibtech promotes a challenging, collaborative, and friendly culture that is centered around our values. and mission.\nDefibtech is supportive of work balance, providing company gatherings to add fun and generous paid time off and flexibility for employees to manage time and responsibilities.\nDefibtech is committed to empowering and supporting our employees in their philanthropic efforts through donation programs and time off for volunteerism.\nThe above description of core responsibilities and qualifications are intended to describe the general nature and level of the work being performed, but they are not an exhaustive list of all the required responsibilities and skills of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.\nDefibtech endeavors to make our application process accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact Human Resources at 203.453.6654. This contact information is for accommodation requests only and should not be used to inquire about the status of applications.\n\n#J-18808-Ljbffr","company":"Defibtech","rawCompany":"defibtech","city":"Brooklyn","state":"NY","isRemote":false,"isActive":true,"createdAt":"2026-08-18T04:05:00.883Z","occupations":[{"code":"17-2112.02","title":"Validation Engineers","slug":"validation-engineers"},{"code":"17-2199.00","title":"Engineers, All Other","slug":"engineers-all-other"},{"code":"17-2031.00","title":"Bioengineers and Biomedical Engineers","slug":"bioengineers-and-biomedical-engineers"}],"industries":[{"code":"334510","title":"Electromedical and Electrotherapeutic Apparatus Manufacturing","slug":"electromedical-and-electrotherapeutic-apparatus-manufacturing"},{"code":"541330","title":"Engineering Services","slug":"engineering-services"},{"code":"334513","title":"Instruments and Related Products Manufacturing for Measuring, Displaying, and Controlling Industrial Process Variables","slug":"instruments-and-related-products-manufacturing-for-measuring-displaying-and-controlling-industrial-process-variables"}],"jobPosting":{"@context":"https://schema.org","@type":"JobPosting","title":"Validation Engineer","description":"Defibtech is seeking a Validation Engineer to join our Research & Development team! This position will be based onsite at our Guilford, Connecticut site, with hybrid flexibility. The Validation Engineer will have primary responsibilities in planning, designing, developing, implementing, and monitoring the validation strategies that support the release of next generation medical devices. In this role, you will function as a cross functional team member developing test protocols based on requirements, documentation, and feedback to impact patient outcomes.\nCore Responsibilities: Supports the development of validation plans for medical device design functions (software, electrical and mechanical), defines appropriate test methods and apply statistical methods to identify sample sizes.\nDevelops and executes validation protocols based on system requirements and approved procedures and standards (ISO and FDA).\nCollates, analyzes, summarizes, and interprets validation protocol results into cohesive reporting for FDA and CE Mark approvals.\nProperly documents activities in accordance with best engineering practices, company procedures, and regulatory requirements.\nParticipates in Design Reviews and provides verification support to development teams (e.g., Code Reviews, Software Module and System testing, test automation, testing procedures).\nDesigns test equipment, test fixtures, and testing software for diagnosis of medical devices.\nDemonstrates Defibtech’s values on the job and promotes and participates in continuous improvement.\nActively supports compliance of Company operations to all applicable laws, regulations and standards, good business practices and company documented procedures (including but not limited to FDA, Quality Management Systems Regulations, safety regulations, and applicable statutes).\nQualifications / Requirements: Bachelor’s degree and 0-2 years of related experience or the equivalent combination of education, experience, and training.\nPreferred candidates will have a bachelor’s degree in a science-related field such as an engineering discipline (e.g., electrical engineering, biomedical, mechanical, and/or computer science) and 2+ years of relevant experience.\nPrevious experience in supporting manufacturing of electronic or electromechanical products in medical device industry, highly preferred.\nPrevious experience working with conventional inspection and measurement equipment, preferred.\nKnowledge of design verification and validation process and practices, preferred.\nKnowledge of engineering design, test, and safety standards (IEC 60601-1 4TH Edition, FDA, ISO), preferred.\nStrong analytical and problem-solving ability.\nStrong technical writing ability for design validations and reports.\nStrong written and oral communication skills to accurately convey issues and information.\nStrong organizational skills and attention to detail.\nAbility to support multiple projects concurrently while maintaining quality and meeting deadlines.\nAbility to work independently and with a team.\nWork Environment and Physical Demands: Work environment is primary based in an office and frequently within an engineering lab setting. Hybrid remote capable.\nPhysical demands are primarily light work which includes sitting as well as frequent walking/standing throughout location(s) and lifting up to 20lbs to carry lightweight test equipment, fixtures, and devices.\nCompensation and Benefits: Defibtech offers competitive salaries and a comprehensive benefits package including core health benefits, company-paid disability, and a company matching 401k plan.\nDefibtech promotes a challenging, collaborative, and friendly culture that is centered around our values. and mission.\nDefibtech is supportive of work balance, providing company gatherings to add fun and generous paid time off and flexibility for employees to manage time and responsibilities.\nDefibtech is committed to empowering and supporting our employees in their philanthropic efforts through donation programs and time off for volunteerism.\nThe above description of core responsibilities and qualifications are intended to describe the general nature and level of the work being performed, but they are not an exhaustive list of all the required responsibilities and skills of this position. Reasonable accommodations may be made to enable individuals with disabilities to perform essential functions.\nDefibtech endeavors to make our application process accessible to all users. If you would like to contact us regarding the accessibility of our website or need assistance completing the application process, please contact Human Resources at 203.453.6654. This contact information is for accommodation requests only and should not be used to inquire about the status of applications.\n\n#J-18808-Ljbffr","datePosted":"2026-08-18T04:05:00.883Z","dateModified":"2026-08-18T04:05:00.883Z","hiringOrganization":{"@type":"Organization","name":"Defibtech","sameAs":"https://jobsearcher.com"},"jobLocation":{"@type":"Place","address":{"@type":"PostalAddress","addressLocality":"Brooklyn","addressRegion":"NY","addressCountry":"US"}},"identifier":{"@type":"PropertyValue","name":"JobSearcher","value":"2c55731b113e3067390ecfb4"},"url":"https://jobsearcher.com/jobs/2c55731b113e3067390ecfb4"}}