Sr. Manufacturing Engineer - Shockwave Medical

Johnson & Johnson Johnson & Johnson · Pharma · Santa Clara, CA +1

This role is for a Sr. Manufacturing Engineer in the medical device industry, focusing on designing, developing, and implementing manufacturing processes, tooling, and fixtures throughout the product lifecycle. It involves collaboration with R&D, QA, and Production, process improvement using Lean principles, and ensuring compliance with quality system requirements.

What you'd actually do

  1. Work collaboratively with R&D, QA and Production departments to design, develop, test, document and implement processes, tooling, and fixtures.
  2. Support and work with Quality to address and resolve non-conformances.
  3. Collect data and analyze process performance and capabilities for company products, including new products and products already in production.
  4. Identify process requirements, advise and support operations management, and implement equipment and fixtures needed for process development and manufacturing efforts.
  5. Develop and maintain documentation for design control, product configurations, manufacturing procedures, lot history records, (e.g., bills-of-materials, MPI’s, LHR’s), and other Quality System requirements.

Skills

Required

  • Bachelor’s degree in Engineering
  • Minimum five (5) years of experience in a medical device environment or 3 years of experience with a master's degree
  • Knowledge of and compliance with applicable Quality System requirements (e.g., traceability QSRs, ISO and MDD requirements)
  • Experience implementing Lean and Lean Sigma concepts
  • Experience with Validation of Medical Devices (IQ-OQ-PQ)
  • Ability to use special software such as: Solidworks, Minitab or related
  • Ability to work in a fast-paced environment while managing multiple priorities
  • Operate as a team and/or independently while demonstrating flexibility to changing requirements.

Nice to have

  • Proficiency in Statistics (Cpk, Hypothesis Testing, DOE, Gage R&R)

What the JD emphasized

  • medical device environment
  • Quality System requirements
  • Validation of Medical Devices (IQ-OQ-PQ)