Staff Clinical Engineer

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are 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 more at

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.

Job Function:

R&D Product Development

Job Sub Function:

R&D Software/Systems Engineering

Job Category:

Scientific/Technology

All Job Posting Locations:

Boston Massachusetts United States of America Raynham Massachusetts United States of America

Job Description:

About Orthopaedics

Fueled by innovation at the intersection of biology and technology were developing the next generation of smarter less invasive more personalized treatments.

Are you passionate about improving and expanding the possibilities of Orthopaedics Ready to join a team thats reimagining how we heal Our Orthopaedics teams help keep more than 6 million people moving each year while delivering clinical and economic value to surgeons and healthcare systems. Our teams build solutions for joint reconstruction; trauma and craniomaxillofacial; sports extremities and elective foot and ankle; spine; and robotics and digital surgery.

Your unique talents will help patients on their journey to wellness. Learn more at are searching for Staff Clinical Engineer to be based out of Boston Massachusetts USA or Raynham Massachusetts with in office expectations of a minimum of 3 days per week.

Purpose:

The Staff Clinical Engineer will work closely with product development teams and clinicians to drive early-stage ideas into high-impact clinically relevant devices and features that redefine surgical robotics and navigation for orthopedics. The Staff Clinical Engineer will accelerate the transfer of breakthrough technologies from concept to clinical application ultimately improving patient outcomes and expanding market leadership. Their primary focus is to provide clinical and technical expertise to inform user needs clinical requirements and real-world performance considerations in order to deliver safe effective and differentiated solutions. This role also supports other cross-functional teams external research institutions and industry partners acting as a catalyst for disruptive innovation and continuous product improvement by providing clinical and scientific expertise throughout the product lifecycle ensuring post-commercial performance meets the design intent.

Job Responsibilities:

• Contribute clinical and technical expertise to the ideation conceptualization and early-stage evaluation of novel design concepts.
• Support projects through feasibility assessment and prototype development ensuring alignment with clinical needs and applicable regulatory pathways.
• Support the preparation and delivery of prototype and product demonstrations for internal stakeholders customers and external partners.
• Collaborate with HEMA marketing R&D and medical affairs to define the patient journey and product maps
• Drive clinical and operational quantitative needs to increase innovation value
• Lead the creation of clinical hazard analyses and procedure-specific risk maps to inform project scope and streamline timelines.
• Stay at the forefront of Computer Assisted Orthopedic Surgery by evaluating emerging trends in surgical robotics other navigated devices and emerging surgical techniques.
• Translate insights into actionable project goals and provide input to prototype development activities that maintain competitive advantage.
• Identify critical tasks potential use errors and hazardous situations in clinical contexts.
• Collaborate with systems engineering to design test methods models and metrics to ensure test protocols and validation activities reflect realistic clinical scenarios and user profiles.
• Analyze clinical workflows environments and pain points to inform system concepts and architecture.
• Conduct observation studies to identify pain points inefficiency and complications.
• Gather Voice of the Clinician (VoC) and clinical insights to help identify unmet clinical needs and translate them into system-level opportunities and requirements.
• Support Voice of Customer sessions with surgeons by preparing session materials and product or prototype demonstrations facilitating structured feedback and documenting actionable clinical insights.
• Collaborate with quality systems and human factors engineering to conduct preclinical formative summative and validation studies throughout the design process.
• Analyze complaints field data and adverse events from aclinical useperspective.
• Support Commercial Education teams in developing and delivering training programs for newly launched products.
• Provide on-site support during initial product commercialization and the escalation of critical performance product complaints.
• Responsible for communicating business-related issues or opportunities to next management level

Qualifications/Requirements:

• Bachelors degree in Mechanical Biomedical Electrical Robotics Engineering or a related technical discipline. Masters or PhD preferred with a focus on medical device development or related fields.
• Experience with surgical robotics and principles of biomechanics.
• Expertise in design validation process development and regulatory compliance.
• Strong problem-solving analytical reasoning and decision-making skills.
• Ability to operate independently within a fast-paced innovative environment.
• Minimum of 7 years in medical device R&D with extensive first-hand experience supporting digital technology in the operating theater early-stage technology incubation innovative device design and development.
• Proven track record of contributing clinical and technical expertise to complex projects from concept evaluation through prototype development initial validation and initial clinical use.
• Demonstrated ability to lead cross-functional teams and manage projects with minimal supervision.
• Strong entrepreneurial mindset with a focus on disruptive innovation and strategic growth.
• Excellent verbal and written communication skills with experience presenting to executive leadership regulatory bodies and external partners. Proven ability to foster collaborative relationships across internal teams and external research institution.
• This position will require significant interactions with customers of J&J field sales leaders and external development partners
• Work closely with Health Care Professionals (Surgeons) to conduct preclinical formative summative and validation studies throughout the design process
• Interactions with Health Care Professionals (Surgeons Clinical Staff) Field Sales Commercial Education and Professional Education administering field based complaint characterization risk assessments and onsite remediation.
• Collaborate with third-party development partners during prototype development by providing clear clinical specifications design inputs and feedback throughout the design process to ensure alignment with clinical technical and business requirements.

Johnson & Johnson announced plans to separate our Orthopaedics business to establish a standalone Orthopaedics company operating as DePuy Synthes. The process of the planned separation is anticipated to be completed within 18 to 24 months subject to legal requirements including consultation with works councils and other employee representative bodies as may be required regulatory approvals and other customary conditions and approvals.

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. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants needs. If you are an individual with a disability and would like to request an accommodation external applicants please contact us via internal employees contact AskGS to be directed to your accommodation resource.

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Required Skills:

Preferred Skills:

Agility Jumps Analytical Reasoning Coaching Collaboration Critical Thinking Model-Based Systems Engineering (MBSE) Product Design Report Writing Requirements Analysis Research and Development SAP Product Lifecycle Management Scripting Languages Software Architectures Software Development Management Software Engineering Practices Software Quality Assurance (SQA) Systems Development Lifecycle (SDLC) Technologically Savvy

The anticipated base pay range for this position is :

$109000.00 - $174800.00

Additional Description for Pay Transparency:

Subject to the terms of their respective plans employees are eligible to participate in the Companys consolidated retirement plan (pension) and savings plan (401(k)).



This position is eligible to participate in the Companys long-term incentive program.



Subject to the terms of their respective policies and date of hire employees are eligible for the following time off benefits:

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 period10 days

Volunteer Leave 32 hours per calendar year

Military Spouse Time-Off 80 hours per calendar year

For additional general information on Company benefits please go to: - Experience:

Staff IC