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 Technical Leader - Medical Devices**
The resource will operate in R&D within the** **Medical Devices Business Unit and will be responsible of the design of components and finished products.
The main tasks will be:
- Support and management for creation of drawings and bill of materials for components and finished products
- Definition and implementation of functional physical tests of the products under development
- Drafting of the product design documentation (**design input, design output, design transfer**)
- Assistance to Production in the development of new projects or sustaining of products already on the market
- Participation in activities related to change control and investigation of complaints
- Collaborate cross functionally leading R&D activities /projects
- Responsible for **Risk Analysis activities** including health hazard assessment, Fault Tree Analysis, Process Failure Mode Control Analysis, Design Failure Mode Control Analysis and **CAPA**:
- Investigate and respond to complaints
- Technical review **Clinical Evaluation Report CER**:
- Responsible for analyze Post-market surveillance report
**Requirements**:
- Product Life Cycle system and Design Control knowledge
- Project Leading skills
- Knowledge of **FDA QSR, ISO13485, ISO 8637-1, ISO14971 and EU Medical Device Directive**:
- Plastics material know how and process technique as injection molding
**Job Offer**
Permanent contract
**Location**
Modena