Regulatory Affairs Specialist - IVDR

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