Principal Research & Development (R&D) Engineer at Treace

Ponte Vedra Beach, Florida, United States -

Full Time

Start Date

Immediate

Expiry Date

12 Aug, 26

Salary

0.0

Posted On

14 May, 26

Experience

10 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

SolidWorks, CAD Design, FEA Simulations, GD&T, ASME Y14.5, Product Development, Design for Manufacturability, Design for Inspection, Risk Assessment, Verification and Validation, Material Selection, Medical Device Design, Project Planning, Prototyping, ISO Standards, Cross-functional Leadership

Industry

Medical Equipment Manufacturing

Description

Company Description Treace’s mission is to be the leader in the surgical treatment of bunions by establishing the Lapiplasty® System as the standard of care. We are committed to operating our business with the highest standards of ethical conduct. We intend to exceed our customers’ expectations through an innovation-driven, high-velocity approach to solving treatment and surgical problems. With our products and services, our mission is to assist foot and ankle surgeons in improving patient outcomes and reducing healthcare costs, while providing rewarding experiences and opportunities for our employees and stakeholders. Job Description Are you a technical expert and innovative leader looking to make a significant impact in product design and development? We are seeking a Principal R&D Engineer to manage and execute key design projects while mentoring other engineers. This role offers the opportunity to lead major product development initiatives from concept to production and contribute to the company’s short-term and long-term goals. Primary Duties & Responsibilities As a Principal R&D Engineer, your responsibilities include: Leading, participating in, and supporting activities throughout product development, including: Concept generation Project planning, design, and execution stages Prototyping, design for manufacturability (DFM), design for inspection (DFI) Risk assessments, pilot production, and design reviews Verification, validation, and testing (protocol authorship, physical testing, reports) Pre-production and full production launch Demonstrating expertise in material selection, manufacturing methods, inspection techniques, and critical measurements. Engaging directly with customers alongside sales and marketing to gather design ideas, document concepts, and transition them into high-quality production-ready products. Ensuring compliance with the company’s design quality system. We're looking for candidates with the following qualifications: Design Expertise - Expert CAD knowledge (preferably SolidWorks) for creating parametric models and ASME Y14.5-compliant prints. Manufacturing Feasibility - Proficient in interacting with design and manufacturing teams to balance manufacturability, reliability, and cost-effectiveness. Analytical and Technical Expertise - Advanced knowledge of CAD design, 3D print generation, FEA simulations, and ISO standards. Communication and Leadership - Strong ability to communicate schedules, budgets, designs, and testing results effectively to teams and stakeholders. Customer-Centric Approach - Ability to generate product designs based on customer input and surgeon feedback. Hands-On Approach - Comfort with cadaver work, surgical settings, and detailed research experiments to test feasibility. Collaborative Team Player - Proven ability to work on cross-functional teams and assist in creating design documentation for medical devices. To excel in this role, you should demonstrate: Exceptional organizational and communication skills. Strong attention to detail. Expertise in product development, material selection, and industry best practices. A desire to work on complex engineering problems and mentor your peers to grow the team’s capabilities. Educational and Software Proficiency Advanced experience using Microsoft Office tools (Word, Excel, PowerPoint, Project). SolidWorks proficiency required; familiarity with FEA and GD&T is a must. Qualifications Bachelor’s degree in Mechanical Engineering or equivalent engineering discipline 7+ years’ mechanical design and manufacturing experience of which 5+ years of actual product development experience bringing innovative product to market from conception to launch in regulated industry. (Preference is given to medical device development). Additional Information All your information will be kept confidential according to EEO guidelines. Treace's Privacy Policy It is Treace’s policy not to discriminate against any applicant for employment, or any employee because of age, color, sex, disability, national origin, race, religion, veteran status or any other characteristic protected by applicable law. EEO/Disabled/Veterans Employer Treace is a drug free employer.

Responsibilities

Lead the end-to-end product development process from concept generation and prototyping to full production launch. Collaborate with customers and surgeons to translate feedback into high-quality, production-ready medical devices.