Software Quality Engineering Lead

Johnson & Johnson Johnson & Johnson · Pharma · Santa Clara, CA +2

Lead Software Quality Engineering role at Johnson & Johnson focused on ensuring compliance and quality for medical device software projects. Responsibilities include managing direct reports, reviewing software deliverables, providing expertise in verification and validation, and collaborating with project teams to meet global standards and regulations.

What you'd actually do

  1. Manage Direct Reports and oversees their medical device software projects to ensure compliance to local procedures and regulatory requirements.
  2. Review project/program software deliverables (e.g. plans, requirements, specifications, test protocols, test cases, test results, traceability, risk management documents, reports).
  3. Provides direction and leadership for verification and validation of non-product software, products software, software tools and components.
  4. Provide expertise in establishing good software requirements, specifications, detailed design, verification and validation protocols and planning documentation.
  5. Collaborate with project/program teams to ensure software deliverable comply with company procedures, global ISO standards (ISO 13485, ISO14971, IEC62304), regulations (e.g. 21 CFR Part 820, 21 CFR Part 11, European Union Medical Device Directive (MDD)/ Medical Device Regulation (MDR), and applicable guidance.

Skills

Required

  • Bachelor's degree in Computer Science, Engineering or related field
  • 8 years of experience in Software Quality Engineering Lead-related occupation
  • Certified Software Quality Engineer (CSQE) certification
  • Project Management Professional (PMP) certification

What the JD emphasized

  • medical device software
  • compliance
  • regulatory requirements
  • ISO 13485
  • ISO14971
  • IEC62304
  • 21 CFR Part 820
  • 21 CFR Part 11
  • European Union Medical Device Directive (MDD)/ Medical Device Regulation (MDR)