Technical Lead, NPI Manufacturing Engineer

Noah Medical

  • San Jose, CA
  • 9 days ago

    Highlights

    Minimum a four-year degree (Bachelor's) in industrial or mechanical engineering or an equivalent combination of education and experience in medical devices with QSR/FDA ISO 13485:2016 or in a highly regulated manufacturing environment. Implement lean manufacturing principles, drive continuous improvement initiatives, and utilize data analytics to streamline ME operations, increase productivity, and reduce cost in processes.

    Numbers & Facts

    LocationSan Jose, CA

    Description

    About You

    • Provide leadership and guidance to the Manufacturing Engineering team (ME) during NPI New Product Introduction through sustaining.
    • Manages ME processes, improvements, and execution of time based deliverables
    • Implement lean manufacturing principles, drive continuous improvement initiatives, and utilize data analytics to streamline ME operations, increase productivity, and reduce cost in processes.
    • Creates and improves processes and procedures for ME and related areas.
    • Excellent theoretical, analytical, and practical skills; appropriately applied to resolving manufacturing issues.
    • Develops and supports effective product field returns strategy and procedures
    • Escalates and resolves design, manufacturability, quality, and supply chain issues
    • Responsible for setting up DMR/DHR/LHR management for a complex system
    • Creates workflow process diagrams, detailed manufacturing and shipping work instructions, procedures, checklists, travelers, product and equipment maintenance plans
    • Develops floor and line layout proposals for build capacity, quality, time optimization and effective inventory management
    • Participates in BOM management, technical specification reviews, new part requisitions
    • Leads process failure mode and analysis (PFMEA) activities
    • Develops and validates critical tests used in production workflow to minimize risk
    • Responsible for the activities of validation and qualification of manufacturing equipment and processes utilizing standard qualification approaches (IQ/OQ/PQ)
    • Manages development and delivery of completed validation plans, studies, and reports
    • Provides feedback for product and process DFM improvements to R&D to ensure optimal manufacturability and serviceability
    • Provides technical support in analyzing and/or performing investigation for discrepant production components, assemblies, and field returns
    • Assists with assembly, testing, and troubleshooting of new products
    • Provides leadership, training, and technical support to production technicians
    • Implements fixtures to aid in production, maintenance, and service
    • Support Good Manufacturing Practices and quality management system in accordance with FDA regulatory and ISO 13485 requirements.
    • Other related duties.

    Qualifications

    • Minimum a four-year degree (Bachelor's) in industrial or mechanical engineering or an equivalent combination of education and experience in medical devices with QSR/FDA ISO 13485:2016 or in a highly regulated manufacturing environment
    • Need a minimum of 5 years of experience in manufacturing engineering of complex electromechanical devices and medical device
    • Must be able to read and understand assembly drawings, BOMs, workflow diagrams, MPIs, and read basic schematics
    • Good written and verbal communication skills with all levels of employees, suppliers, and internal customers
    • Demonstrates ability to grow in career

    #LI-Onsite

    Similar Jobs