Quality Engineer II

Atec Spine

  • Carlsbad, CA
  • 30+ days ago

    Highlights

    Develop, improve, and implement quality methods and systems, working on cross functional teams in a regulated environment to ensure the safety, reliability and efficacy of products and processes. Lead Material Review Board (MRB), own Non-Conformance (NC) development and resolution, lead reworks and deviations, participate in Supplier Review Board (SRB).

    Numbers & Facts

    LocationCarlsbad, CA

    Description

    Mechanical Quality Engineer supporting new product development. Develop, improve, and implement quality methods and systems, working on cross functional teams in a regulated environment to ensure the safety, reliability and efficacy of products and processes.

    Essential Duties and Responsibilities

    • Support New Product Development as primary QE for mechanical implants and instruments. Manage multiple concurrent major and minor projects.
    • Support Design Controls to ensure efficient, effective, and compliant new product launches.
    • Support the qualification of legal manufacturers (OEM) for distributed products.
    • Lead Material Review Board (MRB), own Non-Conformance (NC) development and resolution, lead reworks and deviations, participate in Supplier Review Board (SRB).
    • Develop inspection plans and custom gauging based upon required measurement and tolerances.
    • Support Change Order review for drawings, considering Design for Manufacturing (DFM) and Design for Inspection (DFI).
    • Act as liaison between supplier and company for quality related concerns or issues. Technical interface with contract manufacturers.
    • Support cleaning and sterilization validations of implantable devices; basic understanding of tests such as bioburden, BET, and dose audit testing.
    • Support validation (IQ, OQ, and PQ) development and execution internally and at suppliers.
    • Apply statistical techniques to analyze manufacturing processes and recommend appropriate process controls.
    • Support Risk Management efforts in accordance with ISO 14971; conduct preliminary risk assessments for projects. Support Failure Mode and Effects Analysis (FMEA) for designs and processes.
    • Support Field Retrieval Assessment (FRA) and Health Hazard Evaluation (HHE) as needed.
    • Support MDSAP, FDA, ISO, and other regulatory audits.
    • Apply external standards and guidance documents to project / product specific application.
    • Own Supplier Corrective Actions (SCARs) and Corrective and Preventive Actions (CAPAs).
    • Lead supplier part qualification for new products including process qualifications (PQs), GR&R, first articles, and process development.

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