R&D Engineer – Medical Devices




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Operations — Engineering/production

Secteur Industriel

Life sciences

Niveau d'expérience

3 à 5 ans


Modena, Emilia Romagna, Italie

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Akkodis, is a global leader in the engineering and R&D market that is leveraging the power of connected data to accelerate innovation and digital transformation.


With a shared passion for technology and talent, 50,000 engineers and digital experts deliver deep cross-sector expertise in 30 countries across North America, EMEA and APAC.


Akkodis offers broad industry experience, and strong know-how in key technology sectors such as mobility, software & technology services, robotics, testing, simulations, data security, AI & data analytics.


The combined IT and engineering expertise brings a unique end-to-end solution offering, with four service lines – Consulting, Solutions, Talents and Academy – to support clients in rethinking their product development and business processes, improve productivity, minimize time to market and shape a smarter and more sustainable tomorrow.


Akkodis is a commercial brand under which both AKKA and Modis entities operate.


With a view to strengthening our team, we are looking for a:



R&D Engineer - Medical Devices



The resource will be part of an R&D team and will provide engineering support for design, development or optimization of medical devices.



The main activities include:


  • Design and Development of non-active plastic medical device in compliance with MDD/MDR standards and 21 CRF Part 820 
  • Design and Development of plastic device involving extrusion molding and welding experience
  • Autonomy drafting and managing project documentation according to Design Control within Medical Device DHF
  • Define and support all laboratory tests with the V&V Team
  • Development of test method and in Test method Validation activities
  • Writing of Technical V&V documentation


The ideal candidate has a degree in Biomedical Engineering, Material Engineering, Chemical Engineering or equivalent and has 2 years of experience. Geographical mobility is required at national and international level. Knowledge of the English language is required.






  • Knowledge of applicable standards for non-active medical device (ISO 13485, MDR, ISO 14971, ISO 11607)
  • Knowledge of applicable standards for preparation and quality management of fluids for haemodialysis (ISO 23500
  • Experience in managing project documentation according to Design Control Process within Medical Device DHF
  • Knowledge and ability to comprehend technical drawings





Permanent Contract






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Notre Politique d’embauche participe à améliorer la représentation de la diversité au sein des effectifs du Groupe AKKA. Nos recrutements sont donc ouverts à tous les candidats dont le profil correspond aux caractéristiques et exigences du poste, en dehors de toute autre considération que les qualités et compétences professionnelles.

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