Senior R&D Engineer

We believe that great healthcare is an essential safeguard of human dignity.At Laborie, we know the work we do matters – it’s what fuels our motivation and contributes to our success. If you’re ready to make a positive impact in the lives of patients across the globe, we’d like to meet you. We support and empower our employees to grow their careers in an environment that encourages a sense of belonging and a connection to doing good. We’re not afraid to roll up our sleeves to make our goals a reality and work together to solve for our customers. We reward and recognize our employees based on our values of Aspire to Greatness, Respect All, Own It, Working Together, Persist with Passion.

About the role

As a key member of the R&D team, the Senior R&D Engineer will work cross functionally to complete product design, new product development, and manufacturing activities for drug coated catheter combination medical devices. Additionally, this position will facilitate transfer to manufacturing activities, process development, and ensure device manufacturing is conducted efficiently according to the company quality system. The position focuses on medical device design and development, molded parts and assemblies, project planning, test method development, process validation, design verification & validation, analysis and reporting.

Responsibilities

• Responsible for activities on new product development and product/process improvement for consumable medical devices (Class I, II, and II) including design, prototyping, material selection, verification and validation, maintaining DHF documentation, and design for manufacturability/manufacturing transfer.
• Assess and define sustaining engineering activities per product line in collaboration with cross functional partners.
• Develop product test methods by studying product requirements; research, design, modify, and test medical devices including combination products.
• Collaborate with manufacturing to identify and qualify equipment vendors.
• Plan, document, and execute design verification and validations. IQ/OQ/PQ, draft protocol/reports, risk management (dFMEA), and statistical data analysis.
• Develop applicable manufacturing documents including MPs, IPs, LHRs, and material handling procedures. Prepare, review, and approve processes, protocols, reports, and other controlled documentation.
• Ensure processes and procedures comply with relevant regulations such as EU MDR, ISO, FDA, etc.