Jobs

    Senior Manufacturing Engineer - International, United States - Michael Page

    Michael Page
    Michael Page International, United States

    3 weeks ago

    Michael Page background
    Full time
    Description

    About Our Client

    My client is a global leader in medical device manufacturing, committed to improving healthcare outcomes worldwide. With a focus on innovation, quality, and patient safety, they design and produce cutting-edge medical devices that meet the highest industry standards.

    Job Description

    The Senior Manufacturing Engineer will report directly into the Manufacturing Engineering Manager and be responsible for:

  • Lead manufacturing process development, optimization, and validation activities for medical device production.
  • Collaborate with cross-functional teams to design and implement manufacturing processes that meet product specifications, quality standards, and regulatory requirements.
  • Identify opportunities for process improvements, cost reduction, and efficiency gains through data analysis and process monitoring.
  • Develop and implement strategies to scale up production and increase manufacturing capacity while maintaining product quality and compliance.
  • Lead root cause analysis and corrective/preventive action (CAPA) activities to address manufacturing issues and ensure product quality and regulatory compliance.
  • Mentor and provide guidance to junior manufacturing engineers and technicians.

    Apply today for immediate consideration

    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.

    The Successful Applicant

  • Bachelors Degree in Biomedical or Mechanical Engineering
  • 8+ years of experience in medical device manufacturing
  • Knowledge of regulatory requirements (ISO 13485)
  • Lean Manufacturing (Six Sigma Green Belt preferred)
  • Proficiency in CAD software (e.g., SolidWorks, AutoCAD)
  • Sound analytical and problem-solving skills
  • Experience with FEA analysis tools is a plus
  • Strong communication skills and ability to work in cross-collaborative teams What's on Offer
  • Competitive compensation
  • Comprehensive benefits plan
  • Career growth opportunities
  • Access to high level management
  • 401K match
  • Excellent work life balance


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