Senior Robotics Verification & Validation Engineering Manager

Johnson & Johnson

Senior Robotics V&V Engineering Manager responsible for ensuring robotic products are compliant and effective. Leading a team in delivering comprehensive verification and validation activities for medical devices.

Posted 6/4/2026full-timeBoston • Massachusetts • 🇺🇸 United StatesSenior💰 $137,000 - $235,750 per yearWebsite

Tech Stack

Tools & technologies

Python

About the role

Key responsibilities & impact

Lead a team of Verification & Validation and Integration Engineers to ensure robotic systems meet all defined subsystem and system level requirements.
Collaborate closely with systems engineering, hardware, and software teams to ensure requirements are clearly defined, testable, and fully 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.
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.
Coordinate and manage engagement with external test facilities (e.g., NRTLs, EMC, and restricted materials laboratories) to ensure full regulatory compliance and adherence to internal company policies.
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.
Communicate business-related issues or opportunities to next management level.
Follow all Company guidelines related to Health, Safety and Environmental practices as applicable.
For those who supervise or manage a staff, ensure that subordinates follow all Company guidelines related to Health, Safety and Environmental practices and that all resources needed to do so are available and in good condition, if applicable.
Ensure personnel and Company compliance with all Federal, State, local and Company regulations, policies, and procedures.
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.
7+ years of experience in V&V engineering within the medical device industry.
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).
Preferred: Experience with Class II or Class III medical devices is preferred.
Knowledge of embedded systems, firmware/software testing, or electromechanical systems is a plus.
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

Subject to the terms of their respective plans, employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).
This position is eligible to participate in the Company’s long-term incentive program.
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.

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

Verification and Validation (V&V)requirements managementtest methods designrisk-based approachtest automationembedded systemsfirmware testingelectromechanical systemsstatistical methodssample size calculation

Soft Skills

communicationtechnical writingproblem solvingteam leadershipcollaborationproject managementroot cause analysisregulatory complianceorganizational skillsinterpersonal skills

Certifications

CQECQASix Sigma