We have a current opportunity for a Regulatory Affairs Specialist - IVDR on a contract basis in Northern Ireland. Please apply if you have the skill set and are interested:
- 6-12 months project
- Full time (39 hours per week)
- Hybrid
- Start - May/June
- IVDR Regulatory Knowledge, getting ready for clinical trials.
- GAP Assessments
- Technical Documents
- IVDR submissions
