Development Engineer - BONESUPPORT
Skånestor ABSammanfattning
Join BONESUPPORT as a Development Engineer in Lund, Sweden, where you will play a key role in designing and developing innovative medical devices. This position involves working through the entire product development process, from concept to manufacturing, with a strong focus on mechanical design and verification. Collaborate with cross-functional teams and external partners to create robust technical solutions that meet regulatory requirements.Jobbet i korthet
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Det här erbjuder vi
Opportunity to contribute to innovative medical device development.Work in a growing company with a focus on product development and engineering expertise.Engage in technical development projects that impact patient care.
Ansök senast: 2026-12-01
Publicerad: 2026-10-30
Beskrivning
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.
To succeed in this role, we believe you have:
A technical academic background at Bachelor's level or higher, preferably in Mechanical Engineering or a related field.
Relevant experience in mechanical design and product development within the medical device industry.
Hands-on experience with 3D CAD software, such as SolidWorks, Inventor or similar.
Experience in creating engineering drawings, technical specifications and detailed design documentation.
Good understanding of materials, manufacturing processes and mechanical design principles.
Experience in planning, performing and documenting design verification activities, including test methods, protocols and reports for mechanical and functional testing.
Knowledge of Design for Manufacturing (DFM), Design for Assembly (DFA) and tolerance analysis.
Ability to analyze technical problems, evaluate test results and develop practical engineering solutions.
Good technical writing and documentation skills.
Preferred qualifications
It is an advantage if you also have experience or knowledge in:
Injection molding, tooling and component manufacturing.
Design Control and requirements management.
Risk management according to ISO 14971.
Usability engineering according to IEC 62366.
Medical device safety standards.
Implantable medical devices.
Statistical methods and test method development.
Design transfer and collaboration with external manufacturing partners.
Personal qualities
We believe you are analytical, structured and solution-oriented, with a strong interest in technical problem-solving and product development.
You enjoy working hands-on with engineering challenges and have the ability to translate technical requirements into practical and reliable design solutions.
You take ownership of your tasks, work independently and proactively drive activities forward. At the same time, you value collaboration and enjoy working with colleagues from different technical and functional backgrounds.
You are comfortable working in an environment where technical challenges require both attention to detail and an understanding of the complete product development process.
Why BONESUPPORT?
At BONESUPPORT, you will have the opportunity to contribute to the development of innovative medical devices that make a difference for patients.
You will join a growing company where product development, engineering and manufacturing expertise come together. The position offers an opportunity to take an active role in technical development projects and contribute to the continued development of BONESUPPORT's products.
Location: Lund, Sweden
Application
SKÅNESTOR is managing the recruitment process on behalf of BONESUPPORT.
Please apply directly through this advertisement. For questions, please contact SKÅNESTOR at maria.gren@skanestor.se.
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.
To succeed in this role, we believe you have:
A technical academic background at Bachelor's level or higher, preferably in Mechanical Engineering or a related field.
Relevant experience in mechanical design and product development within the medical device industry.
Hands-on experience with 3D CAD software, such as SolidWorks, Inventor or similar.
Experience in creating engineering drawings, technical specifications and detailed design documentation.
Good understanding of materials, manufacturing processes and mechanical design principles.
Experience in planning, performing and documenting design verification activities, including test methods, protocols and reports for mechanical and functional testing.
Knowledge of Design for Manufacturing (DFM), Design for Assembly (DFA) and tolerance analysis.
Ability to analyze technical problems, evaluate test results and develop practical engineering solutions.
Good technical writing and documentation skills.
Preferred qualifications
It is an advantage if you also have experience or knowledge in:
Injection molding, tooling and component manufacturing.
Design Control and requirements management.
Risk management according to ISO 14971.
Usability engineering according to IEC 62366.
Medical device safety standards.
Implantable medical devices.
Statistical methods and test method development.
Design transfer and collaboration with external manufacturing partners.
Personal qualities
We believe you are analytical, structured and solution-oriented, with a strong interest in technical problem-solving and product development.
You enjoy working hands-on with engineering challenges and have the ability to translate technical requirements into practical and reliable design solutions.
You take ownership of your tasks, work independently and proactively drive activities forward. At the same time, you value collaboration and enjoy working with colleagues from different technical and functional backgrounds.
You are comfortable working in an environment where technical challenges require both attention to detail and an understanding of the complete product development process.
Why BONESUPPORT?
At BONESUPPORT, you will have the opportunity to contribute to the development of innovative medical devices that make a difference for patients.
You will join a growing company where product development, engineering and manufacturing expertise come together. The position offers an opportunity to take an active role in technical development projects and contribute to the continued development of BONESUPPORT's products.
Location: Lund, Sweden
Application
SKÅNESTOR is managing the recruitment process on behalf of BONESUPPORT.
Please apply directly through this advertisement. For questions, please contact SKÅNESTOR at maria.gren@skanestor.se.
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Development Engineer - BONESUPPORT
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