Electronics Manufacturing Engineer II

Johnson & Johnson Johnson & Johnson · Pharma · Danvers, MA +1

Electronics Manufacturing Engineer II at Johnson & Johnson focused on improving and sustaining electronics manufacturing processes for life-saving medical devices. Responsibilities include root cause analysis, process improvement using Lean/Six Sigma, and yield/efficiency enhancement. Requires a Bachelor's degree in engineering and experience in a regulated industry.

What you'd actually do

  1. Root Cause Analysis: Use project root cause analysis tools and techniques to solve opportunities. Ensure timely and effective resolution of owned nonconformance investigations. Address and resolve manufacturing stoppages that require heightened focus. Perform engineering sample runs and testing, and author engineering summaries to support product disposition.
  2. Process Improvement: Support qualification and process validation efforts for relevant system level-testing. Own and support CAPA actions to prevent future non-conformances. Implement Lean Manufacturing and Six Sigma principles to streamline workflows and reduce waste. Work closely with production teams to identify and address process bottlenecks. Reports status on assigned projects in various formats to various organizational levels. Ensures that project plans are comprehensively reviewed, implemented, and completed on schedule and within budget.
  3. Yield and Efficiency Improvement: Edit and summarize production data into broadly understandable terms to communicate project progress with leadership. Find opportunities for reducing scrap and rework. Develop and implement strategies to improve product yield and overall production efficiency. Collaborate with multi-functional teams to address root causes of yield issues and implement sustainable solutions.

Skills

Required

  • Bachelor's degree in mechanical engineering, electrical engineering, or equivalent experience
  • 1-4 years engineering experience in a regulated industry
  • Proven problem-solving skills and a data-driven approach to decision-making
  • Experience with nonconformance management and investigation
  • Experience with CAPA and process validation (IQ/OQ/PQ) projects
  • Effective communication and collaboration skills

Nice to have

  • Experience within the medical device industry
  • Has supported or led successful yield improvement and process optimization projects
  • Experience with electromechanical production processes or capital equipment
  • Experience with project management and release of medical devices within a regulated environment

What the JD emphasized

  • regulated industry
  • nonconformance management and investigation
  • CAPA and process validation (IQ/OQ/PQ) projects
  • regulated environment