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Medical Device Technician

Job

VIVOS Professional Services, LLC

Madison, WI (In Person)

Full-Time

Posted 6 days ago (Updated 16 hours ago) • Actively hiring

Expires 8/6/2026

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Job Description

Medical Device Technician at VIVOS Professional Services, LLC Medical Device Technician at VIVOS Professional Services, LLC in Madison, Wisconsin Posted in 4 days ago.
Type:
full-time
Job Description:
Medical Device Technician Location:
Madison, WI Position Summary We are seeking a Medical Device Technician to support the assembly, testing, troubleshooting, and repair of medical device products and accessories in a regulated manufacturing environment. The ideal candidate will have experience working with technical assemblies, strong problem-solving abilities, and a commitment to quality and compliance. Key Responsibilities Assemble, test, troubleshoot, and repair medical device products and subassemblies following work instructions and SOPs. Perform diagnostics and corrective actions on product performance issues. Maintain accurate production and quality documentation in compliance with company and regulatory requirements. Support equipment maintenance and ensure production readiness. Communicate quality, equipment, or process concerns to Supervisors, Team Leads, Quality, and Engineering teams. Assist with the development and revision of SOPs, Work Instructions, Device History Records, and related documentation. Train and support production team members as needed. Maintain a clean, organized, and safe work environment. Adhere to GMP, quality system, EHS, and regulatory requirements. Participate in continuous improvement initiatives and process enhancements. Perform additional duties as assigned. Qualifications Required Bachelor's degree in Engineering, Life Sciences, or a related technical field; OR Associate's degree with 2+ years of relevant experience; OR High School Diploma/GED with 6+ years of manufacturing or technical assembly experience. Strong troubleshooting, problem-solving, and process improvement skills. Ability to work independently and meet production deadlines. Excellent attention to detail and documentation practices. Preferred Experience in medical device, pharmaceutical, or cGMP-regulated manufacturing environments. Knowledge of controlled documentation systems. SAP experience. Lean Manufacturing and/or Six Sigma certification or experience. Additional Information This role requires advanced troubleshooting and diagnostic capabilities and frequent collaboration with Manufacturing, Materials, Quality, and Engineering teams to support production objectives and continuous improvement efforts.