Product Development Engineer
restor3d
- Durham, NC
- $70,000-80,000 per year
- Permanent
- Full-time
- Supporting the design and engineering efforts for company products, which may include, but is not limited to:
- Developing clinical use understanding of restor3d & market research through literature and interactions with internal team & surgeon design teams
- Researching current surgical techniques and design considerations
- Modeling implant, instrument (drivers, depth gauges, drill guides, etc.), and fixture 3D CAD models/drawings using modeling software (SolidWorks)
- Printing metal and polymer prototypes
- Identifying feasibility and verification testing requirements and conducting testing
- Documenting the design process in accordance with company quality procedures including development plans, design inputs & outputs, drawings, labeling, risk documentation, verification & validation plans/reports, and regulatory submission items
- Collaborating with operations, manufacturing engineers, and suppliers to support new product development and sustaining efforts
- Developing and managing project timelines for line extensions and sustaining engineering efforts
- Working with the commercial team to support launch strategy and forecasting
- Performs other related duties as assigned
- Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, or equivalent Engineering
- Experience with 3D modeling software (Solidworks, ProE, 3-matic, Fusion360, Rhino, etc.)
- Ability to read and understand scholarly journal articles
- Independent worker willing to learn and develop necessary design, manufacturing, and software skills though guided trainings and self-guided research
- Self-starter willing to take ownership of assigned projects and action items
- Previous experience within medical device industry strongly preferred
- Knowledge of human anatomy (through coursework or training)
- Understanding of working under a quality management system for medical devices
- Demonstrated ability of working with design control activities and verification & validation activities in medical device development (ISO 13485 and FDA 21 CFR 820)
- Familiarity with orthopedic implant field
- Experience with basic hand tools, 3D printers, materials testing frames, cleaning and inspection equipment
- CSWA certification
- Ability to work flexible hours, if necessary