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Staff Clinical Engineer
Johnson & Johnson. Contribute clinical and technical expertise to ideation, conceptualization, and early-stage evaluation of novel design concepts .
Posted 9/23/2026full-timeBoston • Massachusetts • United StatesLead💰 $109,000 - $174,800 per yearWebsite
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in medical device development, particularly in surgical robotics and design validation, while effectively collaborating with cross-functional teams to drive innovation and ensure regulatory compliance.
Highest-signal resume keywords
Surgical RoboticsDesign ValidationRegulatory ComplianceMedical Device R&DProject Management
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Mechanical EngineeringBiomedical EngineeringElectrical EngineeringRobotics EngineeringProcess DevelopmentClinical Hazard AnalysisPrototype DevelopmentAnalytical ReasoningDecision-MakingClinical Workflow Analysis
Soft Skills
Problem-SolvingCommunicationCollaborationLeadershipFacilitation
Tools & Technologies
Computer-Assisted Orthopedic SurgerySurgical TechniquesValidation StudiesDigital Technology
Industry Keywords
Medical Device DevelopmentClinical InsightsVoice of the ClinicianVoice of CustomerInnovation Value
About the role
Key responsibilities & impact- Contribute clinical and technical expertise to ideation, conceptualization, and early-stage evaluation of novel design concepts
- Support feasibility assessments and prototype development aligned with clinical needs and regulatory pathways
- Prepare and deliver prototype and product demonstrations for internal stakeholders, customers, and external partners
- Collaborate with HEMA, marketing, R&D, and medical affairs to define patient journeys and product maps
- Drive clinical and operational quantitative needs to increase innovation value
- Lead clinical hazard analyses and procedure-specific risk maps
- Evaluate emerging trends in computer-assisted orthopedic surgery, surgical robotics, navigated devices, and surgical techniques
- Translate clinical insights into project goals and prototype development inputs
- Identify critical tasks, potential use errors, and hazardous clinical situations
- Collaborate with systems engineering to design test methods, models, metrics, protocols, and validation activities
- Analyze clinical workflows, environments, and pain points to inform system concepts and architecture
- Conduct observation studies and gather Voice of the Clinician insights
- Support Voice of Customer sessions with surgeons through preparation, facilitation, demonstrations, and documentation
- Collaborate with quality, systems, and human factors engineering on preclinical, formative, summative, and validation studies
- Analyze complaints, field data, and adverse events from a clinical-use perspective
- Support Commercial Education teams in developing and delivering product training
- Provide on-site support during initial product commercialization and escalation of critical performance complaints
- Communicate business-related issues or opportunities to the next management level
Requirements
What you’ll need- Bachelor’s degree in Mechanical, Biomedical, Electrical, Robotics Engineering, or a related technical discipline
- Master’s 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
- Minimum of 7+ years in medical device R&D
- Extensive firsthand experience supporting digital technology in the operating theater, early-stage technology incubation, innovative device design, and development
- Proven track record 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 problem-solving, analytical reasoning, and decision-making skills
- Excellent verbal and written communication skills
- Experience presenting to executive leadership, regulatory bodies, and external partners
- Ability to foster collaborative relationships across internal teams and external research institutions
- Significant interaction with J&J customers, field sales leaders, and external development partners
- Ability to work closely with surgeons and clinical staff on preclinical, formative, summative, and validation studies
- Ability to collaborate with third-party development partners using clinical specifications, design inputs, and feedback
Benefits
Comp & perks- Pension plan
- 401(k) savings plan
- Long-term incentive program
- Vacation – 120 hours per calendar year
- Sick time – 40 hours per calendar year (Colorado: 48 hours; Washington: 56 hours)
- 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