Principal Test Engineer

Johnson & JohnsonWest Chester, PA
Onsite

About The Position

The Principal Test Engineer provides technical leadership and subject matter expertise in biomechanical and functional testing, research, and computer modeling and simulation of orthopedic implants and instrumentation. The role requires staying current with advances in orthopedic surgery, biomechanics as well as assessing emerging testing technologies and developing innovative test methods to translate complex biomechanical scenarios into representative mechanical test procedures. Additionally, strong investigative and research skills are required to support clinical relevance.

Requirements

  • Minimum of a Master’s degree or equivalent in Mechanical Engineering, Materials Science, Electrical Engineering, Biomedical Engineering, or a related discipline
  • Minimum of 8 years of experience in the medical device industry
  • Minimum of 4 years of experience with servo-hydraulic and electromechanical test equipment and/or modeling and simulation (e.g., Ansys, Abaqus, or similar tools)
  • Experience with data processing and statistical analysis
  • Experience with technical writing
  • Knowledge of Good Laboratory Practice (GLP)
  • Knowledge of Good Documentation Practice (GDP)
  • Strong verbal and written communication skills
  • Technical writing proficiency
  • Basic statistical knowledge
  • Strong problem analysis and problem-solving skills
  • Project management capabilities
  • Ability to effectively manage and prioritize multiple tasks

Nice To Haves

  • Good understanding of experimental design; hands-on laboratory experience is a plus
  • Familiarity with CAD software, such as Siemens NX (Unigraphics) or Creo Parametric
  • Knowledge of current ASTM/ISO test standards
  • Knowledge of regulatory guidelines
  • Knowledge of ISO 17025 accreditation

Responsibilities

  • Design and execute experimental testing and simulation protocols for product performance, reliability, and quality
  • Develop and advance test methods and/or simulation workflows to support design optimization, regulatory submissions, technical reports, and marketing materials
  • Act as a mentor and technical leader for engineers and technicians in the functional testing group and across R&D teams
  • Actively participate in standards development (e.g. ASTM, ISO) and industry conferences for orthopedic devices
  • Develop and implement standardized test procedures
  • Generate intellectual property (IP) and publications to support product launches
  • Participate in cross-functional projects
  • Practice and promote good practices and rigor in research techniques, record keeping, and documentation in order to comply with internal and external quality standards/requirements
  • Communicate and escalate business-related issues or opportunities to management or stakeholders
  • Follow all company guidelines related to Health, Safety, and Environmental practices, ensuring that all required resources are available and in good condition, where applicable
  • Ensure personal and company compliance with all federal, state, local, and company regulations, policies, and procedures
  • Perform other assigned duties as needed
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