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Quality Engineering Technician II

Resonetics - Circle Pines, MN

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Job Description

Since 2015, Resonetics has been growing rapidly. Through targeted acquisitions and greenfield investments, we have expanded into a global leader in advanced engineering, prototyping, product development, and micromanufacturing. Each of our locations is focused on specific manufacturing capabilities and technologies that provide a unique solution for the medical device and advanced diagnostic industries.Th Quality Engineering Technician provides inspection support for final and incoming inspection of contract manufacturing materials. Inspection processes include visual and dimensional inspection, review of manufacturing and supplier documentation, and tensile testing. Provides assistance with customer and factor-facing quality support for contract manufacturing of medical device components. Assist with supporting the interface between Resonetics and customers' supplier quality organization, assisting with transition and sustaining of laser micromanufacturing processes, and support for supplier quality management.2nd shift hours: 2pm-10pm Monday-FridayInspecting final documentation packagesConducting incoming inspection of raw materialWorking on continual improvement projects as assignedAssist with customer quality personnel to resolve issues and Customer ComplaintsGenerating process deviations, Customer Change Notices, validation protocols & reportsAssisting with troubleshooting of production processesAssisting with PReP process activitiesMaintain the calibration and maintenance programsAssist with developing and maintaining quality/control plansAssist with developing PFMECAsConducting Gage R&R studiesWork with Quality Systems to resolve Corrective and Preventive ActionsDocument Nonconformance dispositions and route for approvalSupport production and validation data analysisOther duties as assignedMinimum 2 years’ experience in a Quality Control roleExperience with measurement equipment and microscope useAbility to work under minimal supervisionCommunication and organizational skillsMedical Device Manufacturing background preferredFamiliarity with ISO and FDA Compliance desirableDemonstrated technical writing skillsAssociates Degree or Equivalent Experience.Primarily light office workMay involve bending and lifting of light to medium weight objects.For temp, temp-to-hire, and regular full-time positions, our company policy is that we are unable to provide visa sponsorship. Candidates must already be legally authorized to work in the United States without the need for sponsorship now or in the future.Thecompensation for this role is competitive and will be based on experience and qualifications. The anticipated range is $20-30/hr

Created: 2026-02-19

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