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Senior Robotics Verification & Validation; V&V Engineer

Job in Boston, Suffolk County, Massachusetts, 02298, USA
Listing for: 6149-DePuy Synthes Products Inc. Legal Entity
Full Time position
Listed on 2026-07-13
Job specializations:
  • Engineering
    Quality Engineering, Test Engineer, Regulatory Compliance Specialist, Systems Engineer
Salary/Wage Range or Industry Benchmark: 120000 - 160000 USD Yearly USD 120000.00 160000.00 YEAR
Job Description & How to Apply Below
Position: Senior Robotics Verification & Validation (V&V) Engineer

Senior Robotics Verification & Validation (V&V) Engineer

Location:

Raynham, MA or Boston, MA. Minimum 3 days in office per week, up to 5 days, travel up to 30%.

Responsibilities
  • Collaborate with systems engineering to ensure requirements clarity, testability, and traceability.
  • Define minimum testable requirements post-change.
  • Develop and execute comprehensive V&V strategies and master system test plans, including investigation, integration, reliability, and formal V&V testing.
  • Prepare and deliver system‑level V&V documentation, including summary reports and verification results.
  • Review and approve subsystem verification deliverables.
  • Design, validate, and implement test methods, including manual and automated test setups.
  • Oversee maintenance of robotics test lab facilities, ensuring equipment calibration and compliance.
  • Ensure compliance with regulatory standards (FDA 21 CFR Part 820, ISO 13485, IEC 60601, ISO 14971).
  • Support design transfer, product launch activities, complaints investigations, and root cause analysis.
  • Interface with regulatory, quality, and manufacturing teams to support audits and inspections.
  • Communicate business‑related issues or opportunities to management.
  • Follow all company guidelines related to Health, Safety and Environmental practices.
Qualifications
  • Bachelor’s or Master’s degree in biomedical engineering, systems engineering, electrical engineering, or related field.
  • 3+ years of V&V engineering experience in the medical device industry.
  • Experience with Class II or Class III medical devices preferred.
  • Knowledge of embedded systems, firmware/software testing, or electromechanical systems.
  • Strong understanding of systems engineering principles and product development lifecycle.
  • 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.
EEO Statement

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, disability, protected veteran status or other characteristics protected by federal, state or local law.

Information on accommodation for individuals with disabilities is available at

#J-18808-Ljbffr
Position Requirements
10+ Years work experience
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