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Johnson & Johnson

Makes prescription drugs and medical devices

Navigation Systems Verification & Validation Engineering Manager

Engineering LeadershipPosted on Nov 11
Full-time

About the Job

Requirements

  • A bachelor's or master's degree in biomedical engineering, systems engineering, electrical engineering, or a related field is required.
  • At least 7 years of Verification & Validation engineering experience in the medical device industry is required.
  • Strong understanding of systems engineering principles and product development lifecycle methods, such as V-model, waterfall, and Agile, is required.
  • Experience with requirements management tools such as DOORS, Jama, or Polarion is required.
  • Familiarity with test automation tools and scripting languages such as Python, LabVIEW, or MATLAB is required.
  • Strong technical writing and communication skills are required.

Responsibilities

  • Lead a team of Verification & Validation and Integration Engineers to ensure navigation systems meet all defined subsystem- and system-level requirements.
  • Collaborate with systems engineering, hardware, and software teams to ensure requirements are clearly defined, testable, and traceable from user needs and system/subsystem requirements through verification and validation.
  • Define minimum testable requirements following design or requirement changes, applying a risk-based approach that considers essential performance and basic safety.
  • Develop and execute comprehensive V&V strategies and master system test plans for complex medical devices, including system verification protocols and regression strategies to ensure robust requirements coverage; oversee investigational, integration, reliability, and formal verification and validation testing.
  • Prepare and deliver system-level V&V documentation, including summary reports and verification results.
  • Review and approve subsystem verification deliverables to ensure alignment with overall system requirements.
  • Design, validate, and implement test methods, including manual and automated test setups, to verify product requirements, including repeatability and reproducibility.
  • Coordinate and manage engagement with external test facilities, including NRTLs, EMC, and restricted-materials laboratories, to ensure regulatory compliance and adherence to internal company policies.
  • Oversee maintenance of navigation systems test lab facilities, ensuring equipment and infrastructure are calibrated, serviced, and compliant with company safety, quality, and procedural standards; proactively identify and resolve issues to support testing and development workflows.
  • Ensure compliance with applicable regulatory standards, including FDA 21 CFR Part 820, ISO 13485, IEC 60601, and ISO 14971.
  • Support design transfer and product launch activities, including complaints investigations.
  • Investigate and document non-conformances, deviations, and test failures; drive root cause analysis and corrective actions.
  • Interface with regulatory, quality, and manufacturing teams to support audits and inspections.
  • Communicate business-related issues or opportunities to the next management level.
  • Follow applicable company guidelines for health, safety, and environmental practices.
  • For staff supervised or managed, ensure subordinates follow company health, safety, and environmental guidelines and that necessary resources are available and in good condition, as applicable.
  • Ensure personal and company compliance with federal, state, local, and company regulations, policies, and procedures.
  • Perform other duties as assigned.
  • Identify critical paths during product development, address bottlenecks and risks, and facilitate problem solving across R&D teams.
  • Support project resource and schedule planning.

Desired Qualifications

  • Experience with Class II or Class III medical devices is preferred.
  • Knowledge of embedded systems, firmware/software testing, or electromechanical systems is a plus.
  • Experience in surgical robotics or surgical navigation technologies is a major plus.
  • Certification in CQE, CQA, or Six Sigma is a plus.
  • Proficiency in sample size calculation and statistical methods for analyzing data is desirable.

About the Company

Johnson & Johnson

Makes prescription drugs and medical devices

Johnson & Johnson develops prescription medicines and makes medical devices for hospitals, and unlike most big drugmakers, it runs both businesses under one roof. In 2015, its Darzalex became the first antibody drug approved for multiple myeloma, a blood cancer. Its medicines treat cancer, immune diseases such as psoriasis, and mental illnesses such as depression, and patented drugs bring in most of its sales. Its MedTech unit makes heart pumps, catheters that treat irregular heartbeats, surgical sutures, and Acuvue contact lenses. It was founded in 1886 to make sterile surgical dressings, is based in New Brunswick, New Jersey, and spun off its consumer brands, such as Tylenol and Band-Aid, as Kenvue in 2023.

Company size
10,001+
Company stage
IPO
Headquarters
New Brunswick, NJ
Founded
1886

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