Job title: In emergency and clinical affairs
Are you an expert in the regulatory and clinical field? Is there an opportunity to develop business and stimulate international projects? We are currently looking for matters and clinical for an Italian company to connect with the orthopedics sector. With more than 20 years of experience in design, production and marketing of orthopedic devices, we have been engaged in orthopedic reconstruction, including the production of hip and knee prosthetic guides, oncology prostheses and artificial limbs. Their fans depend on the dedication to having major production presence in their productions. Moreover, in the three years he recorded 30% dismissals.
benefits:
- You will have the opportunity to work for a company with a great reputation and complete control over product quality and innovation.
- You will participate in stimulating and dynamic projects, providing you with professional development and growth.
- You will be part of an experienced team and collaborate with passionate professionals in the field of orthopedic surgery.
Responsibilities:
- Manage branches independently or with support from the CRO, mainly covering MDR 2017/745 and original commission principles.
- Joint communication with ethics committees and judicial authorities to obtain advanced image licenses.
- Implementation of the post-market surveillance system under MDR 2017/745 including reporting and report writing.
Requirements:
- Rules table knowledge of MDR 2017/745 and subsequent amendments and the original MDCG of the commission.
- Experience managing details and communicating with ethics committees and judicial authorities.
- Ability to write design and evaluation reports for medical devices according to MEDDEV 2.7.1. review. 4 guidelines.