Product Development Engineer III

Job Summary

Product Development Engineer III applies advanced engineering principles and medical device product development expertise to develop and support Surgical Navigation products from concept through commercialization. This role is responsible for planning and executing engineering activities within our product development process, including design documentation, verification and validation, prototype and production-intent builds, and cross-functional project execution.

Job Duties And Responsibilities

• Translate customer, user, and clinical needs into product requirements, engineering specifications, and design inputs.
• Perform concept development, feasibility assessments, risk analyses, and design reviews.
• Collaborate with both our external customers and internal Quality, Regulatory, Operations, Commercial Team and Supply Chain teams to ensure product requirements are met while maintaining compliance with design control and quality system requirements.
• Troubleshoot complex technical challenges and drive effective resolutions.
• Evaluate design alternatives and implement solutions that optimize performance, reliability, manufacturability, and usability.
• Support Voice of Customer (VOC) activities and apply market and clinical insights to product development.
• Ensure compliance with applicable medical device regulations, design controls, risk management processes, and quality system requirements.

Engineering Documentation

• Create and maintain engineering documentation including CAD models, drawings, GD&T specifications, BOMs, product specifications, test protocols, test reports, and DHF deliverables.
• Support design verification and validation activities through timely and thorough documentation.

Design Verification & Validation

• Develop and execute verification and validation strategies, plans, protocols, and reports.
• Define test methods, acceptance criteria, and data collection approaches to demonstrate compliance with product requirements.
• Analyze test results, resolve identified issues, and present findings during technical and design reviews.

Verification & Validation Builds

• Coordinate prototype, engineering, and production-intent builds.
• Partner with Operations, Manufacturing Engineering, Supply Chain, and Quality to ensure build readiness and successful execution.
• Track build outcomes, document findings, and drive issue resolution.

Cross-Functional Collaboration

• Collaborate with Quality, Regulatory, Clinical, Marketing, Manufacturing, Supply Chain, Program Management, and Operations teams to achieve project objectives.
• Support design transfer, manufacturing readiness, and product launch activities.
• Communicate project status, technical risks, and mitigation plans to stakeholders.
• Contribute to continuous improvement initiatives that enhance product quality and development efficiency.

Qualifications

• Bachelor's degree in Mechanical Engineering, Biomedical Engineering, or a related engineering discipline.
• 5+ years of product development experience, preferably in the medical device industry.
• Experience developing mechanical and/or electromechanical products in a regulated environment.
• Strong knowledge of design controls, risk management, and regulated product development processes.
• Expertise in product design, DFx, materials selection, manufacturing processes, and mechanical problem-solving.
• Experience creating engineering documentation, including drawings, specifications, BOMs, DHF deliverables, and verification/validation documentation.
• Proficiency with SolidWorks or similar 3D CAD software, including GD&T and engineering drawing creation.
• Experience with prototyping, verification and validation testing, root-cause analysis, and technical troubleshooting.
• Strong technical writing, analytical, and problem-solving skills.
• Proficiency with Microsoft Office Suite.
• Able to independently manage technical work and collaborate effectively within cross-functional teams.
• Experience supporting FDA submissions, including 510(k) and/or PMA programs.

Preferred Experience

• Experience developing Surgical Navigation, image-guided surgery, or capital medical equipment products.
• Medical device manufacturing experience.
• Knowledge of FDA QSR, ISO 13485, IEC 60601, and other applicable medical device standards.
• Experience supporting design transfer and manufacturing readiness.
• Experience with machine shop operations, injection molding, and additive manufacturing.
• Familiarity with requirements management, FMEA, statistical analysis, Microsoft Project, and Minitab.

EEO Statement

Forj Medical provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state or local laws. This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation and training.

Compensation And Total Rewards Package

The salary range for this position is outlined below under "Job Details" and is dependent upon the individual's skills, experience, qualifications, and applicable employment laws. Beyond base salary, Forj offers a competitive Total Rewards Package. We offer health, dental, vision, 401K plans, and time off programs. You may also be eligible to participate in an annual bonus program which depends on various factors, including, individual and organizational performance.