What You’ll Do: Interface with surgeons and sales representatives to gather input for design and evaluation of product enhancements and sustaining projects Utilize advanced knowledge of surgical procedures to develop innovative solutions that meet customer needs Independently design, develop, modify, evaluate, and verify mechanical components and subsystems for medical devices Lead large projects and actively participate on cross-functional design teams (R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing, and Project Management) Participate in and lead design reviews as applicable Lead creation and refinement of engineering documentation, including Design History Files, Change Control, Nonconformance & CAPA records, and Regulatory Technical documentation Translate user needs into design inputs and specifications and produce complex system-level designs Conduct advanced prototyping and testing; develop fixtures for verification testing as needed Analyze and correct complex product design issues using independent judgment Support Voice of Customer sessions internally and with clinicians Prepare and review information for invention disclosures and patent applications Mentor others on industry standards, design requirements, test strategies, design controls, risk management, and change control per the Quality Management System Identify and support improvements to procedures, policies, processes, systems, and technology Apply knowledge of materials, manufacturing processes, and Design for Manufacturability (DFM) principles Deliver high-quality results while collaborating across teams to achieve business objectives What You Bring: Bachelor of Science in Mechanical Engineering, Biomedical Engineering, or related discipline (Master’s preferred) 4+ years of relevant work experience Strong technical ability to develop and optimize designs for mechanical assemblies incorporating DFM principles High proficiency with parametric CAD packages (Creo or SolidWorks preferred) and strong skills in creating engineering drawings, models, GD&T, and CAE tools Adept at applying knowledge of materials and manufacturing processes to product design High level of experience and demonstrated proficiency with design controls within a regulated industry Moderate project management skills, including building timelines and budgets and monitoring progress Ability to communicate moderate-complexity plans and technical information clearly Ability to work with a low level of supervision while providing moderate strategic and tactical input Responsible for leading large projects Why VB Spine? We believe in growing talent from within. At VB Spine, join a high-performing R&D team where you’ll play a critical role in sustaining and evolving innovative spinal implants and instruments that improve patient lives. Compensation: Pay for this role is competitive and based on experience, qualifications, and performance. The typical pay range for this position is $115,000.00 - $125,000.00 annually, with potential for bonuses and incentives plus benefits. Final compensation is determined on a case-by-case basis and considers a variety of factors including experience level, technical expertise, and market conditions. Benefits include: Comprehensive health, dental, and vision insurance 401(k) with company match Paid time off (PTO) and holidays Ongoing training and professional development opportunities Opportunity to grow within a fast-paced, dynamic company Staff Engineer Location: Leesburg, VA or Allendale, NJ Company: VB Spine Looking for a career where your work truly matters? At VB Spine, you’ll be part of a mission-focused team that supports surgeons during life-changing spinal procedures. We’re the largest privately held spine company and among the largest family-owned medical technology companies in the world, dedicated to innovation, surgeon partnerships, and improving patient outcomes in spine care. As a Staff Engineer in our R&D function within the Spine division, you’ll perform complex implant and instrument design work, lead large projects, and actively participate on multi-functional teams to advance sustaining projects for commercially available products — including product evolution, regulatory documentation updates, and supply chain continuity.