Principal Engineer, R&D

How you'll make an impact:

• Lead in improving, designing, and optimizing more complex tests, analyzing results, providing recommendations, and developing reports based on engineering principles that translate to innovative products.
• Support project teams to optimize device design and performance by utilizing design tools and predictive engineering methods (e.g., CAD, FEA, and optimization)
• Analyze and evaluate experimental data to create and validate the computational models.
• Present the analysis results to the stakeholders and contribute to publishing internal reports and technical summaries.
• Proactively identify issues, achieve resolution, and resolve problems of significant complexity in designing parts, components, and subsystems
• Work in a cross-functional team environment and collaborate with R&D, Regulatory, Quality, Manufacturing, and Supply Chain to meet project objectives.
• Some domestic and international travel (up to 5%)

What you'll need (Required):

• Bachelor's degree in engineering or Scientific field, with 6 years' experience, including either industry or industry/education - OR -
• Master's Degree or equivalent in Engineering or Scientific field, with 5+ years' experience, including either industry or industry/education - OR -
• Ph.D. or equivalent in Engineering or Scientific field, with 2+ years' experience, including either industry or industry/education

What else we look for (Preferred):

• MS or PhD degree in materials science or mechanical engineering is preferred.
• 2+ years of experience in engineering design
• 2+ years of experience in structural, Mechanical, or Fatigue Analysis
• Demonstrated proficiency in nonlinear mechanics, plasticity, and advanced computational modeling techniques (FEA)
• Understanding of general engineering design principles and a working knowledge of the design of experiments (DOE) and other engineering workflows
• Familiarity with the mechanics of soft tissues is a plus.
• Experience with scripting environments such as Python and MATLAB.
• Ability to interact professionally with all organizational levels.
• Ability to manage competing priorities in a fast-paced environment.
• Strict attention to detail.
• Excellent documentation and communication skills and interpersonal relationship skills, including high discretion/judgment in decision-making.
• Knowledge of the cGMP Manufacturing environment within the Medical Device Industry, including knowledge of FDA / TUV guidelines and quality system regulations in general.
• Ability to interact professionally with all organizational levels and proactively escalate issues to appropriate levels of management.
• Participate and present at meetings with internal and external representatives.
• Develop peer, cross-functional, and cross-business relationships to maximize best practice sharing and team effectiveness.
• Ability to work independently without close supervision.