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Team Lead IV, Second Shift

Job in Danvers, Essex County, Massachusetts, 01923, USA
Listing for: Medtronic plc
Full Time position
Listed on 2026-10-22
Job specializations:
  • Manufacturing / Production
    Production QC/QA, Production Manager, Manufacturing & Industrial Operations, Lean Manufacturing / Six Sigma
Salary/Wage Range or Industry Benchmark: 53600 - 80400 USD Yearly USD 53600.00 80400.00 YEAR
Job Description & How to Apply Below

We anticipate the application window for this opening will close on - 2 Nov 2026

Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact.

A

Day in the Life As a Team Lead IV supporting the production of Sen Sight

This position combines hands‑on manufacturing expertise with floor leadership, helping ensure production goals, quality standards, and safety expectations are achieved while supporting the successful development and commercialization of next‑generation medical technologies. Working closely with supervisors, engineers, quality partners, and production teams, you will coordinate workflow, resolve production challenges, support new product builds, and foster a culture of continuous improvement in a dynamic manufacturing environment.

This is a fully onsite position, working a second shift schedule (M‑F 2:30 PM – 11:15 PM).

Responsibilities
  • Lead daily manufacturing operations, coordinating production activities to meet build schedules and program milestones.
  • Prioritize operator assignments based on production schedules, staffing levels, and changing business needs.
  • Preform all transactions within SAP to order materials needed for production and confirm tracking through completion.
  • Provide day‑to‑day leadership, technical guidance, and support to production operators and assemblers while fostering a collaborative and inclusive team environment.
  • Coach and mentor team members on manufacturing processes, standard work, equipment operation, troubleshooting, and problem‑solving techniques.
  • Perform technical reviews and assist with equipment setup, changeovers, testing, disassembly, reassembly, and manufacturing support activities.
  • Monitor production flow and proactively identify opportunities to improve safety, quality, efficiency, and productivity.
  • Communicate production status, process issues, equipment concerns, and schedule updates to supervisors and cross‑functional partners.
  • Support daily operational activities including manufacturing, shipping, inventory management, material movement, and production support.
  • Ensure all products are manufactured in accordance with approved procedures, quality requirements, and regulatory standards.
  • Champion compliance with Medtronic's Quality Management System, Good Manufacturing Practices (GMP), and Environmental Health & Safety (EHS) requirements.
  • Assist with onboarding and training new employees while reinforcing standard work and operational excellence.
  • Participate in continuous improvement initiatives that enhance manufacturing performance, reduce waste, and improve product quality.
  • Support additional operational responsibilities and special projects as assigned.
Required Qualifications
  • 5+ years of related experience
Preferred Qualifications
  • Demonstrated experience leading work, coordinating production activities, or serving as a technical resource within a manufacturing team.
  • Proficient with SAP.
  • Strong understanding of manufacturing processes, quality systems, and safe work practices.
  • Ability to troubleshoot production issues and make sound decisions in a fast‑paced environment.
  • Strong communication, organizational, and interpersonal skills.
  • Proficiency using standard computer applications and production documentation systems.
  • Experience in a regulated manufacturing environment such as medical device, pharmaceutical, biotechnology, or other highly regulated…
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