Device Lifecycle Engineer Co-op

Johnson & Johnson Johnson & Johnson · Pharma · Titusville, NJ +1

Co-op role for a Device Lifecycle Engineer focusing on the device constituents of combination products within the JJIM network. Responsibilities include lifecycle engineering, technical support, and leading product/process quality improvement and reliability projects, ensuring compliance with regulatory standards.

What you'd actually do

  1. Well-documented design change control processes that may include assessments, risk analyses, and implementation plans.
  2. Detailed documentation demonstrating compliance with regulatory standards, including effective technical assessment reports.

Skills

Required

  • Effective problem-solving to assess supplier changes to commercial products within multi-functional teams.
  • Excellent organizational and planning skills, able to balance multiple priorities.
  • Shown ability to respond to complex inquiries from all levels of employees or external sources, strong communication and interpersonal skills.
  • Technical writing skills to efficiently document device design control.
  • Awareness of and willingness to learn medical device regulatory and quality system requirements.
  • Strong interpersonal and decision-making skills, ability to operate with professionalism, confidentiality and in a dynamic environment.
  • Intermediate to advanced digital literacy, including document management systems, word processing, spreadsheets, project planning, and database applications.

Nice to have

  • Experience working within a quality system, experience in the medical industry, or syringe manufacturing/engineering experience.

What the JD emphasized

  • medical device regulatory and quality system requirements