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Skills
Biomedical Engineeringunmatched
Change Controlunmatched
Compensation Managementunmatched
Compensation and Benefitsunmatched
Corrective and Preventative Action (CAPA) Systemsunmatched
Design Evaluationunmatched
Documentationunmatched
Engineering Drawingunmatched
Implantsunmatched
Industry Standardsunmatched
Invention Disclosuresunmatched
Invention Reviewsunmatched
Laboratory Analysisunmatched
Manufacturing Methodsunmatched
Manufacturing Requirementsunmatched
Marketingunmatched
Mechanical Engineeringunmatched
Medical Equipmentunmatched
Microsoft Visual Basicunmatched
PTC Creounmatched
Patent Applicationsunmatched
Patient Careunmatched
Problem Solving Skillsunmatched
Product Designunmatched
Project/Program Managementunmatched
Prototypingunmatched
Quality Managementunmatched
Regulationsunmatched
Regulatory Requirementsunmatched
Requirements Managementunmatched
Research & Development (R&D)unmatched
Risk Managementunmatched
Root Cause Analysisunmatched
SolidWorksunmatched
Statisticsunmatched
Team Playerunmatched
Technical Writingunmatched
Test Benchunmatched
Test Strategyunmatched
Description
What You’ll Do:
Interface with surgeons to gather input for designs and evaluation of new and existing products
Collaborate with R&D, Quality, Manufacturing, Regulatory, Clinical, Marketing, and Project Management teams (with supervision) to ensure project success
Design, develop, modify, evaluate, and verify components for medical devices under supervision
Participate in and support cadaver labs to evaluate designs and ensure user needs are met
Create and refine engineering documentation, including Design History Files, Change Control records, Nonconformance & CAPA documentation, and Regulatory Technical files
Learn and apply R&D procedures such as design controls, risk management, and change control per the Quality Management System
Assist with prototyping, bench testing, and support problem-solving and root cause analysis
Prepare and review information for invention disclosures and patent applications
Participate in design reviews
Develop foundational knowledge of industry standards, design requirements, and test strategies aligned with regulatory requirements
Demonstrate ownership, integrity, and collaborative relationships while managing priorities
What You Bring:
Bachelor of Science in Mechanical Engineering, Biomedical Engineering, or related discipline (Master’s preferred)
1+ year of experience (medical device industry preferred); Co-Op or Internship experience preferred
Basic experience with a parametric CAD package (Creo or SolidWorks preferred)
Fundamental knowledge of mechanical engineering practices, design principles, materials, and manufacturing methods (traditional and additive)
Ability to read and interpret complex engineering drawings
Basic knowledge of analysis tools and statistical methods
Strong willingness to learn, take ownership, and work effectively under supervision
Ability to set and manage personal priorities in a regulated environment
Why VB Spine? We believe in growing talent from within. At VB Spine, join a high-performing R&D team where you’ll gain valuable hands-on experience supporting the evolution and sustainment of 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 $85,000.00 - $95,000.00 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 background, 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