Staff Quality Engineer - Quality Lcm

Johnson & Johnson Johnson & Johnson · Pharma · Irvine, CA +1

Staff Quality Engineer role at Johnson & Johnson (Biosense Webster, Inc.) focusing on quality assurance projects throughout the lifecycle of medical devices (electrophysiology catheters, cables, and systems). Responsibilities include serving as a subject matter expert on Quality LCM, using Quality Engineering tools, collaborating with various departments, leading design verification tests and process validations, ensuring compliance with regulatory standards (FDA, ISO 13485, CMDCAS, PMDA), and utilizing statistical tools for data analysis and process improvement (Six Sigma, SPC, DOE). The role also involves assisting Regulatory Affairs and participating in design reviews.

What you'd actually do

  1. Plan and coordinate quality assurance projects and activities throughout lifecycle of BWI's products, primarily electrophysiology catheters, cables, and systems.
  2. Serve as subject matter expert on Quality LCM (Life Cycle Management) matters.
  3. Use Quality Engineering tools/processes in the development and implementation of practices for effective and efficient development, transfer, and maintenance of products, including manufacturing transfers, project management, shelf life evaluations, and compliance.
  4. Collaborate with QE-NPD, R&D, PMNPD, Operations/Supply Chain, BWI-Israel and other inter- and intra -departmental groups as needed in conducting functional role.
  5. Lead and support design verification tests, process validations, and quality processes to ensure compliance with the company’s Quality System policies and procedures, as well as applicable external regulatory agency requirements and standards, including FDA, ISO 13485, CMDCAS, and PMDA as pertains to medical devices.

Skills

Required

  • Master's degree in Mechanical Engineering, Biomedical Engineering, or related field
  • 4 years of experience in Staff Quality Engineer - Quality LCM-related occupation
  • Quality LCM
  • Quality Engineering tools/processes
  • Design verification tests
  • Process validations
  • FDA, ISO 13485, CMDCAS, and PMDA compliance
  • Statistical tools
  • Six Sigma
  • SPC
  • DOE

What the JD emphasized

  • FDA
  • ISO 13485
  • CMDCAS
  • PMDA