Medical Device Laboratory TechnicianThis role is part of a high-performance cross-functional team responsible for routine particulate testing of medical devices to ensure the highest quality results. The position is ideal for a highly motivated individual who thrives in a fast-paced, regulated environment, demonstrates strong documentation practices, and maintains exceptional attention to detail while supporting patient safety and product quality.ResponsibilitiesPerform routine medical device particulate testing assignments, applying basic interpretation of established procedures to ensure accurate and reliable results.Gather and record test data with strong adherence to good documentation practices, analyze results, verify findings, and prepare clear and accurate test reports.Exercise broad judgment in troubleshooting test issues and equipment problems, escalating and resolving them in a timely manner.Create, maintain, and organize data files, forms, and test documentation to support traceability and compliance requirements.Communicate effectively with a wide range of personnel within and outside the plant to coordinate testing activities and share information.Identify opportunities for improvement in testing processes and participate in continuous improvement projects to enhance efficiency and quality.Use documentation systems to research information, generate change requests, and support updates to procedures and test methods.Assist in developing and qualifying data sheets, equipment fixtures, visual standards, and test methods used in laboratory testing.Initiate, investigate, and assist in the generation and completion of quality-related records and deviation documentation, ensuring thorough follow-up.Assist with product failure analysis by performing tests, gathering data, and contributing to root cause investigations.Communicate testing results clearly and promptly to project teams, engineers, and other stakeholders.Support engineers in failure analysis and corrective and preventive action (CAPA) activities, including serving as a CAPA project team member when assigned.Support process and product qualification activities by executing test protocols and documenting results in accordance with regulatory requirements.Serve in support roles during external audits, including acting as a document retriever and auditee, and ensuring readiness of test documentation.Perform special quality initiatives under guidance, contributing to projects that enhance product and process quality.Consistently demonstrate a primary commitment to patient safety and product quality by maintaining compliance with documented quality policies, processes, and procedures.Employ basic analytical laboratory skills, such as reading a meniscus, pipetting accurately, using a balance, and operating a stir plate and other lab equipment.Operate and maintain test equipment to ensure proper function, calibration, and reliability for ongoing testing activities.Essential SkillsAssociate degree (AA) or equivalent work experience in a related discipline, with 3+ years of related experience.Prior experience working in a laboratory environment, including hands-on analytical laboratory skills such as weighing, pipetting, and applying the scientific method.Ability to perform analytical testing with strong attention to detail and accuracy.Experience using basic measurement tools such as calipers.Chemistry and biology experience relevant to laboratory testing and medical device evaluation.Knowledge and practical use of Microsoft Office applications, including Word, Excel, and Outlook.DV test protocol training and execution experience in a regulated environment.Strong problem-solving skills with the ability to troubleshoot test methods and equipment issues.Ability to quickly learn and follow current test processes and procedures in a regulated setting.Ability to multitask and manage multiple projects at different stages of development.Demonstrated experience analyzing and fulfilling documentation requirements, including compliance with quality standards.Ability to communicate detailed technical and testing information clearly to project teams and stakeholders.Ability to work effectively in a team environment, collaborating with engineers and technicians.Prior experience in test documentation through laboratory notebooks or formal reports.Experience in the medical device industry, preferably with direct involvement in testing medical devices.Ability to operate and maintain laboratory test equipment reliably and safely.Physical ability to lift up to 35 pounds as part of routine laboratory activities.Ability to stand for up to 8 hours during testing and laboratory work.Additional Skills & QualificationsExperience participating in continuous improvement initiatives within a laboratory or manufacturing environment.Familiarity with quality systems, CAPA processes, and deviation documentation in a regulated industry.Comfort working with documentation systems to research information and generate change requests.Experience supporting external audits by retrieving documents and responding to auditor questions.Strong attention to detail and commitment to good documentation practices in all testing activities.Ability to clearly document and communicate failure analysis findings and test outcomes.Willingness to take on special quality initiatives under guidance and contribute to broader quality and process improvement goals.Work EnvironmentThis position operates in a regulated medical device laboratory and manufacturing environment on a standard business first shift, typically from 8:00 AM to 4:30 PM.
The role involves routine use of analytical lab equipment such as pipettes, balances, stir plates, calipers, and other test fixtures, along with regular use of Microsoft Office software for documentation and reporting. Work is primarily performed standing at laboratory benches for extended periods, and the role requires the physical ability to lift up to 35 pounds. The environment is fast-paced and quality-focused, with close collaboration among engineers, technicians, and cross-functional team members. Employees follow established safety and quality procedures and use appropriate laboratory attire suitable for a controlled testing environment.Job Type & LocationThis is a Contract to Hire position based out of Maple Grove, MN.Pay and BenefitsThe pay range for this position is $19.00 - $24.00/hr.Eligibility requirements apply to some benefits and may depend on your job classification and length of employment.
Benefits are subject to change and may be subject to specific elections, plan, or program terms. If eligible, the benefits available for this temporary role may include the following: • Medical, dental & vision • Critical Illness, Accident, and Hospital • 401(k) Retirement Plan – Pre-tax and Roth post-tax contributions available • Life Insurance (Voluntary Life & AD&D for the employee and dependents) • Short and long-term disability • Health Spending Account (HSA) • Transportation benefits • Employee Assistance Program • Time Off/Leave (PTO, Vacation or Sick Leave)Workplace TypeThis is a fully onsite position in Maple Grove, MN.Application DeadlineThis position is anticipated to close on Aug 17, 2026.