Freelance Regulatory Affairs Consultant - IVD Expert | Remote based (EMEA, APAC or US)

To work for a Medical Device consultancy, responsible for global operations. We are looking for a someone to provide Regulatory Affairs consulting services within the IVD space.

What will you be responsible for?
- Regulatory consultancy
- IVDR transition and implementation
- Pre-submission and clinical strategy support
- Clinical Evaluation Plans
- Technical Documents
- Hosting conferences & delivering presentations

Experience?
- Laboratory and/or manufacturing background
- IVD expert (High consultant level)
- IVD Directive (IVDD) to IVD Regulation (IVDR) transition and implementation