Antal International Network
Location
Crema (CR) | Italy
Job description
- Define and document medical devices development according to internal procedures and Design Control requirements.
- Develop new product concepts collecting and analyzing input from clinical, marketing, literature and other sources.
- Review and/or define new product and component requirements.
- Review and/or define new component specification.
- Develop test methods and equipment/fixtures.
- Coordinate technical team for the realization and preparation of bill of materials, verification of adequate components availability, verification of supplier capacity, coordination with production to evaluate feasibility.
- Release and review project documentation (test protocols, test record and test reports).
- Support Product Interface documentation release acting Product Interface Manager role.
- Support internal interfaces (Quality and Production department).
- Support material procurement and shipping requests.
- Monitoring of suppliers concerning status of project and dealing with technical issues.
JOB REQUIREMENTS
- Degree or similar education level in bio-engineering/mechanical engineering discipline.
- 2 (two) years of experience in the Medical devices industry.
- Good knowledge of the English language.
- Ability to take decisions in daily work.
- Basic in technical drawing.
- Basic knowledge about plastic materials and relative manufacturing and assembly technologies.
- Basic knowledge of passive medical devices made in plastic materials.
- Basic knowledge about plastic materials and relative manufacturing and assembly technologies.
- Willingness to travel.
LOCATION: Crema (CR)
Please send your CV with a motivation letter to the role to: [email protected]
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