Our client is one of the world's leading Medical Device companies. Due to continuous expansion, a new position for a Regulatory Affairs Specialist has arisen at their Co. Limerick facility.

**WORK FROM HOME POSSIBILITIES**

The Position:

• Compile and communicate regulatory requirements.
• Prepare and present gap analysis assessments of regulations and guidance to peers and cross-functional groups.
• Review and approve the project documentation (design reports, labelling, etc.).
• Develop tactics supporting first to market commercial opportunities and minimise time to product launch.
• Input to the development of regulatory strategies and provide guidance and expertise.

The Person:

• 3+ Years' experience (Medical Devices preferred).
• Experience of regulatory submissions with exposure to programmable electrical equipment an advantage.
• Knowledge and experience on EU MDR / EU MDD and standards.

Benefits:

• Attractive package on offer for the successful candidate.

To learn more about this role apply online or contact Anna Carey on +353 873928655 or for a confidential discussion.