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Johnson & Johnson

Senior Robotics V&V Engineer

Johnson & Johnson

Senior Robotics V&V Engineer ensuring compliance and safety of robotic medical devices. Collaborating across teams for regulatory submissions and comprehensive V&V activities.

Posted 7/29/2026full-timeBoston • Massachusetts • 🇺🇸 United StatesSenior💰 $92,000 - $148,350 per yearWebsite

Core Competencies

Role fit
Core Competencies

Use this summary to align your resume positioning with the role.

Demonstrates expertise in Verification and Validation (V&V) strategies for complex medical devices, ensuring compliance with regulatory standards and effective communication across multidisciplinary teams. Proficient in requirements management and statistical analysis to support product development and quality assurance.

Highest-signal resume keywords
Verification And Validation EngineeringMedical Device Industry ExperienceRequirements Management ToolsRegulatory Compliance (FDA, ISO)Test Automation Tools

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills
Verification Protocol DevelopmentTest Method DesignStatistical AnalysisEmbedded Systems TestingFirmware/Software Testing
Soft Skills
Technical WritingCommunication SkillsProblem Solving
Tools & Technologies
DOORSJamaPolarionPythonLabVIEWMATLAB
Certifications & Qualifications
CQECQASix Sigma
Industry Keywords
Biomedical EngineeringSystems EngineeringClass II Medical DevicesClass III Medical DevicesProduct Development Lifecycle

Tech Stack

Tools & technologies
Python

About the role

Key responsibilities & impact
  • Collaborate with systems engineering to ensure requirements clarity, testability, and traceability from user needs, system and sub-system requirements, through verification and validation.
  • Define minimum testable requirements post-change (risk-based, essential performance, basic safety).
  • Develop and execute comprehensive V&V strategies and master system test plans for complex medical devices, including system verification protocols and regression plans that ensure robust requirements coverage; this includes investigational, integration, reliability, and formal V&V testing.
  • Prepare and deliver system-level V&V documentation, including summary reports and verification results.
  • Reviewing and approving sub-system verification deliverables to ensure alignment with overall system requirements.
  • Design, validate, and implement test methods, including manual and automated test setups.
  • Oversee the maintenance of robotics test lab facilities, ensuring all equipment is properly calibrated, serviced, and compliant with company safety, quality, and procedural standards.
  • Ensure compliance with regulatory standards (e.g., FDA 21 CFR Part 820, ISO 13485, IEC 60601, 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.
  • Responsible for communicating business-related issues or opportunities to next management level.
  • Identify critical paths during product development, address bottlenecks and risks and facilitate problem solving across R&D teams.
  • Support project resource and schedule planning.

Requirements

What you’ll need
  • Bachelor’s or master’s degree in biomedical engineering, Systems Engineering, Electrical Engineering, or related field.
  • 3+ years of experience in V&V engineering within the medical device industry.
  • Experience with Class II or Class III medical devices is preferred.
  • Knowledge of embedded systems, firmware/software testing, or electromechanical systems is a plus.
  • Strong understanding of systems engineering principles and product development lifecycle (e.g., V-model, waterfall, Agile).
  • Experience with requirements management tools (e.g., DOORS, Jama, Polarion).
  • Familiarity with test automation tools and scripting languages (e.g., Python, LabVIEW, MATLAB).
  • Excellent technical writing and communication skills.
  • Certification in CQE, CQA, or Six Sigma is a plus.
  • Proficient in sample size calculation and statistical methods for analyzing data.

Benefits

Comp & perks
  • Health insurance
  • 401(k) matching
  • Vacation –120 hours per calendar year
  • Sick time - 40 hours per calendar year
  • Holiday pay, including Floating Holidays –13 days per calendar year
  • Work, Personal and Family Time - up to 40 hours per calendar year
  • Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
  • Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
  • Caregiver Leave – 80 hours in a 52-week rolling period
  • Volunteer Leave – 32 hours per calendar year
  • Military Spouse Time-Off – 80 hours per calendar year