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.

Requirements

• 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

Contract

Permanent Contract

Location

Modena