Experienced Engineer Manufacturing Quality

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

Experienced Manufacturing Quality Engineer at Johnson & Johnson (Abiomed) in Danvers, MA. This role focuses on ensuring quality standards in the development and manufacturing of life-saving medical devices, involving compliance with regulations, process validation, risk management, and quality system support. Requires 2-4 years of experience in manufacturing/operations and knowledge of risk management (FDA/ISO).

What you'd actually do

  1. Provide quality engineering support in the development and manufacturing of new and existing medical devices.
  2. Ensure compliance of manufacturing processes and areas to all applicable quality system regulations.
  3. Lead Quality reporting such as, key performance metrics, goals, and objectives.
  4. Lead and support activities related to the Material Review Board.
  5. Lead non-conformance investigations, including cause analysis, documenting findings, and approving material dispositions. Promptly address any quality concerns through corrections, corrective/preventative actions, and Escalations.

Skills

Required

  • Manufacturing/Operations experience
  • Product/process Risk Management (FDA and ISO standards)
  • Risk mitigation implementation
  • Manufacturing equipment and processes technical understanding

Nice to have

  • FDA and European regulatory environment experience
  • Hands-on troubleshooting and problem solving
  • Quick thinking and sound judgment
  • GMP/ISO regulations and validation regulations understanding
  • Project management and project leadership abilities

What the JD emphasized

  • In-depth knowledge of product/process Risk Management (FDA and ISO standards)
  • Experience with a proven track record of implementing appropriate risk mitigation
  • A thorough understanding of GMP/ISO regulations and validation regulations