Development Engineer – BONESUPPORT

Development Engineer – BONESUPPORT

Come and join BONESUPPORT as Development Engineer! This is an opportunity to take an active role in the design and development of innovative medical devices, from early concepts to finalized products and manufacturing.

BONESUPPORT is an innovative and growing medical device company based in Lund, Sweden. The company develops and commercializes injectable bio-ceramic bone graft substitutes for the treatment of bone disorders.

To further strengthen our Development & Engineering department, we are now looking for a Development Engineer with a strong technical background and hands-on experience in mechanical design, product development and verification.

Your role

As Development Engineer, you will be involved in the development of new medical devices as well as improvements to existing products.

You will work throughout the product development process, from concept development and mechanical design to verification, validation and transfer to manufacturing.

The role has a strong technical focus, combining hands-on mechanical engineering and CAD design with testing, material selection and manufacturing considerations. You will be responsible for developing robust technical solutions that meet functional requirements and can be efficiently manufactured.

You will work closely with colleagues within R&D, Operations, Quality Assurance and Regulatory Affairs, as well as external suppliers and manufacturing partners.

Your main responsibilities will include

• Design and develop medical device components and assemblies using 3D CAD tools.
• Execute design activities through all product development phases.
• Create and maintain engineering drawings, technical specifications and design documentation.
• Perform mechanical design activities, including material selection, tolerance analysis and component optimization.
• Develop technical solutions with consideration for Design for Manufacturing (DFM), Design for Assembly (DFA) and Design for Reliability.
• Collaborate with suppliers and manufacturing partners on tooling, injection molding and manufacturing optimization.
• Develop, plan and perform verification and validation testing.
• Establish test methods and prepare test protocols and reports.
• Analyze test results, identify potential improvements and provide recommendations for design modifications.
• Participate in design reviews, risk management activities and cross-functional development projects.
• Support design transfer activities and contribute to design control documentation in accordance with applicable regulatory requirements.

Qualifications

We are looking for a technically skilled engineer with practical experience in mechanical design and product development within the medical device industry.