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Manufacturing Team Lead - Medical Device - Tilton, NH - Tilton New Hampshire

Company: Michael Page
Location: Tilton, New Hampshire
Posted On: 05/03/2024

In this Manufacturing Team Lead role you will be responsible for overseeing production operations within the medical device manufacturing sector. The successful candidate will lead a team of dedicated engineers to ensure the efficient and timely production of high-quality medical devices while adhering to strict regulatory requirements. Client Details My client is a global CMO in the Medical Equipment Manufacturing industry. From concept to commercialization, my client offers end-to-end capabilities to help bring their customers' medical technology solutions to life. Description The Manufacturing Team Lead will report directly into the Engineering Manager and be responsible for:

  • Lead, motivate, and develop a team of approximately six (five manufacturing engineers and one technician).
  • Collaborate with cross-functional teams including engineering, quality assurance, and supply chain to drive continuous improvement initiatives.
  • Monitor production processes and implement corrective actions to address deviations and optimize efficiency.
  • Plan, develop and execute process and test method validation (IQ/OQ/PQ).
  • Ensure compliance with regulatory standards such as ISO 9001, ISO 13485, and FDA regulations.
  • Drive initiatives to reduce waste, improve productivity, and enhance overall operational efficiency.
  • Maintain accurate production records, documentation, and reports as required by regulatory authorities.
  • Provide regular performance feedback, coaching, and training to team members to foster a culture of continuous learning and development. Apply today for immediate consideration! Profile
    • Bachelors Degree in Engineering (Masters in Engineering or MBA is a plus)
    • 5-7+ years of experience in a contract manufacturing industry (Medical Device preferred)
    • Knowledge of continuous improvement, lean and six sigma tools (greenbelt preferred)
    • Working knowledge of ISO 9001, ISO 13485 and FDA regulations
    • Strong communication skills and ability to work in cross-collaborative teams
    • Ability to prioritize tasks, solve problems, and make sound decisions in a fast-paced environment
    • Demonstrated ability to lead and develop a diverse team of professionals Job Offer
      • Competitive compensation
      • Comprehensive benefits plan
      • Career growth opportunities
      • Access to high level management
      • 401K match
      • Excellent work life balance MPI does not discriminate on the basis of race, color, religion, sex, sexual orientation, gender identity or expression, national origin, age, disability, veteran status, marital status, or based on an individual's status in any group or class protected by applicable federal, state or local law. MPI encourages applications from minorities, women, the disabled, protected veterans and all other qualified applicants. More...

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