Medical Device QA/RA SME
Medical Device QA/RASME
Our client is a Medical Device organization that manufactures Implantable Radiation Devices (Brachytherapy) for the treatment of localized cancers. They are currently looking for a Quality Assurance & Regulatory Affairs SME to come on-site and support EU product registrations, as well as day-to-day CAPA activities.
This consultant will be responsible for supporting the QA/RA groups, and will be focusing on product registrations within the EU. The consultant absolutely needs experience with Implantable Radiation Devices (Brachytherapy), and should be aware that this is a radiation facility. This individual will also be responsible for driving CAPA creation and closure for our client.
- Medical Device
- Implantable Radiation Devices (Brachytherapy Products)
- Nuclear Medicine/Radiopharmaceuticals
- EU Product Registrations
Job Type: Contract