Manufacturing Engineer II

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

Manufacturing Engineer II role focused on process improvement, root cause analysis, and yield optimization within a regulated healthcare manufacturing environment. Requires a Bachelor's degree in engineering and 2-5 years of experience in manufacturing engineering, with strong problem-solving and data-driven decision-making skills. Experience with nonconformance management, CAPA, and process validation is essential.

What you'd actually do

  1. Lead and collaborate with team members to ensure timely and effective resolution of 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. Lead initiatives to optimize existing manufacturing processes, focusing quality improvements and efficiency. Own and lead 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.
  3. Analyze manufacturing processes to 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
  • 2-5 years experience in manufacturing engineering in a regulated industry
  • Excellent problem-solving skills
  • 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 teamwork skills

What the JD emphasized

  • regulated industry
  • nonconformance management and investigation
  • CAPA
  • process validation