Senior Robotics V&V Engineer

Johnson & Johnson

Senior Robotics V&V Engineer responsible for validating robotic products in alignment with healthcare standards. Collaborating cross-functionally to support product development and regulatory compliance.

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

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Verification and Validation (V&V) engineering for medical devices, with a strong focus on regulatory compliance, systems engineering principles, and effective communication. Proficient in developing test strategies and managing requirements throughout the product development lifecycle.

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

V&V StrategiesTest 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, to ensure they are suitable for verifying product requirements, including repeatability, reproducibility.
Oversee the maintenance of robotics test lab facilities, ensuring all equipment and infrastructure are properly calibrated, serviced, and compliant with company safety, quality, and procedural standards; proactively identify and resolve issues to support uninterrupted testing and development workflows.
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.
Responsible for following all Company guidelines related to Health, Safety and Environmental practices as applicable.
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; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 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
10 days Volunteer Leave – 32 hours per calendar year
Military Spouse Time-Off – 80 hours per calendar year