Design Quality Engineer

more-jobs; Le Noirmont; Vor Ort; CHF 110.000 - 140.000; Vollzeit

Benefits dieser Stelle

Supportive environment

Family-oriented structure

Innovative and fast-growing SME

Learning and professional development

Zusammenfassung

Bien-Air Surgery in Switzerland (Le Noirmont) seeks a Design Quality Engineer to lead design quality activities, support NPD and design changes, and ensure compliance with MDR, FDA/ISO standards. You will collaborate with multiple departments and contribute to robust design documentation.

The role requires a Bachelor’s in engineering, 1–3 years in medical devices QA, knowledge of DMR/DHF, ISO 13485 and EU MDR. Proficiency in French and English preferred; strong organizational skills.

Qualifikationen

• Bachelor's degree in mechanical, micro-mechanical or biomedical engineering.
• 1–3 years’ experience in quality assurance of medical devices, ideally class IIa or above.
• Demonstrated knowledge of DMR and DHF structure and contents.
• Experience with ISO 13485 QMS and with Risk Management for Medical Devices.
• Experience with EU MDR 2017/745.

Aufgaben

• Lead and support New Product Development (NPD) and Design Changes by ensuring compliance of activities and documentation to internal QMS requirements as well as to external regulations and standards (FDA, ISO).
• Support Verification & Validation activities to ensure compliance with applicable Design Control requirements.
• Generate and maintain Risk Management during NPD and Design Changes using principles from ISO 14971.
• Ensure quality assurance according to principles of Design Changes of medical devices during all stages of product development.
• Update existing product documentation in compliance with requirements of MDR.
• Create, review or approve DMR and DHF documentation released during NPD and Design Changes.
• Contribute to generate and maintain User Information Material.
• Contribute to continuous improvement of internal procedures related to NPD, Design Change and Risk Management.
• Become key contributor to product reprocessing methodology and testing (cleaning and sterilization).

Kenntnisse

Quality assurance

Regulatory knowledge

Documentation control

NPD

Design changes

Ausbildung

Bachelor's degree in mechanical, micro-mechanical or biomedical engineering

Tools

MS Office

PLM system

Jobbeschreibung

Design Quality Engineer

Bien-Air Surgery is a growing international company which develops, manufactures and markets high-tech instruments for microsurgery. We have held an enviable position in the international market for many years thanks to our emphasis on invention and innovation, and the high quality of our products and services.

To support our growth,we are looking to add to our team at our site in B ienn e a:

In this role, you will play a key part in a fast-moving team and participate in the development of our Medical Devices. You will work closely with different departments to ensure the design quality of the final product.

Your Responsibilities:

• Lead and support New Product Development (NPD) and Design Changes by ensuring compliance of activities and documentation to internal QMS requirements as well as to external regulations and standards (FDA, ISO).
  
• Support Verification & Validation activities to ensure compliance with applicable Design Control requirements.
  
• Generate and maintain Risk Management during NPD and Design Changes using principles from ISO 14971.
  
• Ensure quality assurance according to principles of Design Changes of medical devices during all stages of product development.
  
• Update existing product documentation in compliance with requirements of MDR.
  
• Create, review or approve DMR and DHF documentation released during NPD and Design Changes.
  
• Contribute to generate and maintain User Information Material.
  
• Contribute to continuous improvement of internal procedures related to NPD, Design Change and Risk Management.
  
• Become key contributor to product reprocessing methodology and testing (cleaning and sterilization).
  

Your Profile:

• At least Bachelor’s Degree in mechanical, micro-mechanical or biomedical engineering.
  
• 1 to 3 years’ experience into quality assurance of medical devices, ideally class lla or above.
  
• Demonstrated knowledge of DMR and DHF structure and contents.
  
• Experience with ISO 13485 QMS and with Risk Management for Medical Devices.
  
• Experience with EU MDR 2017/745.
  
• Computer skills: MS-Office suite, and ideally PLM system.
  
• Fluent in French, with good knowledge of English (level B2 or higher).
  
• Strong organizational and follow-up skills, attention to detail.
  
• Open-minded personality with the ability to quickly integrate a team.
  

What We Also Offer :

• A supportive and collaborative work environment within a family-oriented company structure.
  
• The opportunity to join an innovative and fast-growing industrial SME.
  
• A role with real impact on the company’s performance and results.
  
• Opportunities for continuous learning and ongoing professional development.
  

• Rue de l'Ouest 2b 2340 Le Noirmont