Senior Device Regulatory Specialist - Global Submissions

1100 Mylan Pharmaceuticals Inc. is seeking a regulatory expert in Dublin to lead and collaborate on regulatory strategies for medical devices and combination products. You will manage Device Program Teams (DPTs) to ensure compliance with FDA and EU regulations while authoring essential documents for regulatory submissions.

The ideal candidate will hold a Bachelor's degree in a scientific field, have experience in the Medical Device industry, and excellent communication skills. We offer benefits including health insurance and a bonus scheme.