Senior Production Lead – Medical Devices

Medtronic

Dexter (AL)

On-site

USD 54,000 - 80,000

Full time

10 days ago
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Job summary

Medtronic seeks a detail-oriented quality professional for its Dexter, MI site to lead production-related inspections and ensure adherence to GDP and regulatory standards. Candidates should bring 5+ years of related experience and demonstrate strength in teamwork, communication, and problem solving.

Responsibilities include coaching operators, managing process issues, and upholding Medtronic quality/safety standards while working on-site with cross-functional teams.

Qualifications

  • Requires 5+ years of related experience.
  • Prior quality/inspection experience preferred.
  • Demonstrated ability to train others on inspections that you are signed off on.
  • Excellent in Good Documentation Practices (GDP).
  • Proven experience of 3-5 years in Quality within a regulated industry such as medical devices or Pharma is required for this role.
  • An ideal candidate should be able to demonstrate a history of strong teamwork, be proficient in problem resolution and skilled in both written and verbal communication.
  • Prior medical device experience.
  • Experience in a clean room environment.
  • Experience with handling and inspecting PCBAs.

Responsibilities

  • Leads production team work processes, equipment testing, manufacturing, disassembly, and reassembly as assigned by supervisor.
  • Prioritizes use of operators according to build schedule.
  • Communicates process issues and provides status updates to teamsupervisor.
  • Coaches operators/assemblers on production and problem solving skills, performing technical review and machinery setup/breakdown as needed.
  • Ensures Medtronic company quality and safety standards are upheld.

Skills

Quality inspection
GDP
Teamwork
Communication
Problem solving

Tools

PCBAs handling

Job description

Medtronic seeks a detail-oriented quality professional for its Dexter, MI site to lead production-related inspections and ensure adherence to GDP and regulatory standards. Candidates should bring 5+ years of related experience and demonstrate strength in teamwork, communication, and problem solving.

Responsibilities include coaching operators, managing process issues, and upholding Medtronic quality/safety standards while working on-site with cross-functional teams.

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