We have an exciting opening at our Westborough, Massachusetts location. Resonetics is searching for a Development Engineer II to join our growing team. This role will be a part of a cross-functional engineering team driving the design, development, verification, and manufacturing transfer of novel interventional medical devices including complex catheters.

Resonetics is a global leader in advanced engineering, prototyping, product development, and micro manufacturing, driving innovation in the medical device industry. With rapid expansion across all our locations, we continue to push the boundaries of technology while fostering a dynamic, employee-centered culture. Our commitment to excellence and continuous improvement makes Resonetics an exciting place for professionals passionate about shaping the future of micro-manufacturing and being part of something bigger.  

• Summarizes and refines product specifications.
• Brainstorms novel therapeutic concepts.
• Performs concept refinement and generates detailed CAD design.
• Prototypes and evaluates catheter-based designs.
• Performs engineering calculations, including tolerance analysis.
• Drafts complex drawings with a demonstrated understanding of component manufacturing methods.
• Develops in-vitro test methods, including fixture design and fabrication.
• Performs in-vivo and in-vitro study protocol development, execution, reporting.
• Develops manufacturing processes and documentation.
• Creates and maintains designs controls documentation.
• Generates product risk analyses.
• Communicates directly with clients in a timely and professional manner.
• Troubleshoots/leads process development activities as needed.
• Maintains a growth mindset by actively seeking and accepting constructive feedback.
• Demonstrates an ability to adapt quickly and positively to changing priorities and processes.
• Incorporates Design for Metrology principles into their work. 
• Routinely incorporates DFM and DFA principles when completing design tasks.
• Demonstrates familiarity and compliance with Quality SOPs. 
• Demonstrates functional application of advanced SolidWorks skills. 

• 1-3+ years' experience in the medical device design/development field.
• Proficient in Microsoft Office: MS Teams, Excel, PowerPoint, Outlook.
• Strong understanding of ISO 13485.
• Experience with SolidWorks.
• Knowledge of materials science and material properties for common medical device materials. 

The compensation for this role is competitive and will be based on experience and qualifications. The anticipated range is $80,000-$87,000.