Systems Verification Engineer
About The Position
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at jnj.com. As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world. We provide an inclusive work environment where each person is considered as an individual. At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.
Requirements
- Master's degree in Electrical, Mechanical, or Computer Systems Engineering or related field and 2 years of experience in the job offered or in a Systems Verification Engineer-related occupation.
- Developing comprehensive test plans that encompass objectives, methodologies, and timelines
- Analyzing specifications and requirements to ensure testing aligns with intended outcomes
- Selecting appropriate testing methods based on timing, cost, accuracy, and other customer requirements
- Analog and digital circuitry, including electrical testing tools
- Creating customized testing equipment and fixtures for specific components or devices
- Python, Linux/Ubuntu and Version control (Bitbucket)
- Leveraging analytical approaches, including statistical analysis and motion analysis
Responsibilities
- Design and lead test method and equipment development, production, and qualification projects for J&J Surgical Robotics system.
- Develop tests, tools, and processes essential to the preparation and execution of design verification.
- Develop tests that holistically verify the safety and efficacy of the Surgical Robotics system.
- Execute equipment qualification, fixture qualification (IQ/OQ), test method validation (Gage R&R), script development, analysis of data, and non-product software validation (NPSW) for design verification.
- Ensure produced test documentation is aligned with FDA design control processes (21 CFR820.30) and IEC 62304.
- Work closely with engineers from all functional teams including R&D (Mechanical, Electrical, Software, Robotics and Control), systems architecture, and quality engineering to guide requirements and product development for testability.
- Develop testing/analysis software scripts in Python, MATLAB, C++, or other scripting languages.
Benefits
- Consolidated retirement plan (pension)
- Savings plan (401(k))
- Long-term incentive program
- Vacation – 120 hours per calendar year
- Sick time - 40 hours per calendar year (may vary by state)
- 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
- Medical insurance
- Dental insurance
- Vision insurance
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
