Manufacturing Supervisor, Third Shift - Minneapolis, MN

MedtronicBrooklyn Center, MN
109d$71,200 - $106,800

About The Position

Join Medtronic Energy and Components Center as a Manufacturing Supervisor, where you'll lead 3rd Shift Production Operations for our high-quality and complex cardiac rhythm management products. In this hands-on leadership role, you will guide a team of 25+ direct labor employees, ensuring operational excellence and supporting both existing and new product lines to meet evolving customer needs. You'll play a key role in driving improvements across safety, quality, delivery, and cost—using your problem-solving skills and the Medtronic Performance System to identify opportunities, develop solutions, and execute strategies that make a real impact. Your ability to foster a culture of collaboration, continuous improvement, and accountability will be vital in supporting Medtronic's mission to alleviate pain, restore health, and extend life.

Requirements

  • Requires high school diploma or GED equivalent.
  • 1+ years of experience in a production or manufacturing role.

Nice To Haves

  • Bachelor's degree and 2+ years of relevant experience; OR Associate's degree and 4+ years of relevant experience; OR High School Diploma/GED and 6+ years of relevant experience.
  • Experience in manufacturing or production environment, preferably in medical device, electronics, or battery manufacturing.
  • Previous leadership or supervisory experience.
  • Strong knowledge of safety, quality, and compliance standards (cGMP, ISO, FDA, etc.).
  • Experience with high rate battery manufacturing processes (e.g., lithium-ion, primary cells).
  • Lean manufacturing or Six Sigma certification.
  • Excellent communication, problem-solving, and organizational skills.
  • Proficiency with production management systems (SAP, MES) and Microsoft Office Suite.

Responsibilities

  • Supervise and coordinate the activities of employees engaged in high rate battery manufacturing, assembly, and testing.
  • Ensure production schedules are met by managing resources, prioritizing work, and resolving issues that may impact output.
  • Foster a culture of safety and compliance, ensuring all team members follow Medtronic's policies and regulatory requirements (e.g., FDA, ISO).
  • Monitor product quality and collaborate with Quality, Engineering, and Maintenance teams to investigate and resolve deviations or non-conformances.
  • Support continuous improvement initiatives; identify opportunities to optimize processes, reduce waste, and increase productivity.
  • Lead, coach, and develop team members through regular feedback, training, and performance reviews.
  • Maintain accurate production records and ensure timely completion of all required documentation.
  • Communicate effectively with cross-functional teams and leadership regarding production status, challenges, and improvement actions.
  • Participate in audits, investigations, and root cause analysis as required.

Benefits

  • Health, Dental and vision insurance
  • Health Savings Account
  • Healthcare Flexible Spending Account
  • Life insurance
  • Long-term disability leave
  • Dependent daycare spending account
  • Tuition assistance/reimbursement
  • Simple Steps (global well-being program)
  • Incentive plans
  • 401(k) plan plus employer contribution and match
  • Short-term disability
  • Paid time off
  • Paid holidays
  • Employee Stock Purchase Plan
  • Employee Assistance Program
  • Non-qualified Retirement Plan Supplement
  • Capital Accumulation Plan

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What This Job Offers

Job Type

Full-time

Career Level

Entry Level

Industry

Miscellaneous Manufacturing

Education Level

High school or GED

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