What are the responsibilities and job description for the Mechanical Engineer position at PathRight Medical Inc.?
Company Description PathRight Medical Inc. designs and manufactures safe, effective, research-backed medical devices for a range of clinical conditions. In collaboration with the Mayo Clinic, the company developed RestoreX, an advanced penile traction therapy device for the treatment of Peyronie’s disease (PD). PathRight Medical emphasizes rigorous clinical validation, quality, and patient outcomes in all product development efforts. Team members work in a focused, mission-driven environment that values innovation and evidence-based solutions.
Role Description This full-time, on-site Mechanical Engineer role is based in Provo, UT. The Mechanical Engineer will contribute to the design, development, and improvement of medical devices, including mechanical components and assemblies. Day-to-day responsibilities include creating and updating CAD models and drawings, performing engineering calculations, supporting prototype builds, and conducting testing and verification activities. The role involves collaborating with cross-functional teams in R&D, quality, and manufacturing to resolve design issues, ensure regulatory compliance, and transfer designs to production. The Mechanical Engineer will also support documentation, participate in project planning, and contribute to continuous improvement of products and processes.
Qualifications
- Strong foundation in Mechanical Engineering with experience in medical devices or related regulated industries.
- Proficiency in Machine Design and mechanical component/assembly design, including tolerance analysis and material selection.
- Hands-on skills with Computer-Aided Design (CAD) tools for 3D modeling and 2D drafting, and experience preparing manufacturing-ready drawings.
- Experience in Research and Development (R&D), including prototyping, testing, data analysis, and design iteration.
- Project Management abilities, such as planning tasks, meeting deadlines, coordinating with cross-functional teams, and maintaining clear documentation.
- Bachelor’s degree in Mechanical Engineering or a closely related discipline; advanced degree is a plus.
- Must have familiarity with medical device standards, quality systems, and regulatory requirements (e.g., ISO 13485, FDA) is beneficial.
- Strong problem-solving skills, attention to detail, and ability to work both independently and collaboratively on-site.