Senior Quality Engineer (npd)

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

Senior Quality Engineer for New Product Development in the medical device industry, focusing on ensuring compliance with GMP, ISO, and other applicable standards throughout the product lifecycle. Responsibilities include developing requirements, verification/validation strategies, risk management, and documentation review.

What you'd actually do

  1. Launch and stabilize new product launches through concept, design, development, and steady-state processes.
  2. Drives the development of product requirements, verification strategies, and validation strategies.
  3. Ensures new product development compliance to GMP (Good Manufacturing Practices), ISO (International Organization for Standardization) and any other applicable standards
  4. Activities would drive prevention, detection of defects at earliest phase of product design, continuous improvement & customer satisfaction.
  5. Proactively engage partners to drive consensus and resolve issues in a timely fashion.

Skills

Required

  • Bachelor’s Degree in Engineering
  • 5 years of quality experience
  • New product development experience
  • GD&T knowledge
  • Experience in medical device industry or other highly regulated field
  • Advanced knowledge of Quality Engineering/Scientific methods and techniques and applied statistics of increasing complexity
  • Team-based environment experience

Nice to have

  • Advanced Degree
  • Experience with medical electrical-mechanical systems
  • Knowledge of FDA requirements for design control of medical devices, particularly with verification and validation of software for medical electrical equipment.
  • ASQ Certified Quality Engineer
  • ASQ Certified Reliability Engineer
  • Green Belt in one or more of the Process Excellence roadmaps (DMADVV, DMAIIC, or Lean)
  • Experience driving risk management discussions
  • Prior software quality engineering experience in a product development environment

What the JD emphasized

  • medical device industry
  • highly regulated field
  • FDA requirements for design control of medical devices
  • verification and validation of software for medical electrical equipment