We are currently recruiting for a Regulatory Analyst role, this has been chosen as job of the week as it is:
- An interesting opportunity to join a well known global leader in the medical device field with a comprehensive portfolio of Orthopaedic and Neurological products
- Responsible for managing and/or coordinating regulatory submissions and files, including 510(k)s, PMAs, PMA supplement, IDE, Minor Modification, EU technical file, design dossier, and technical file revisions as well as providing technical expertise and training in regulatory submissions and regulatory strategy
- The company is based in a great location outside of Cork in a Hub of Pharmaceutical companies. There are great transport links as well as an airport nearby.
- Contract role for 12 months offering an hourly rate between 35-42 Euros/hr