Reg Affairs Specialist II| Perm | Cork | Med Device| MDR | For a confidential discussion and more information on the role, please contact Aisling on 021 4809118 or email firstname.lastname@example.org
My client, a leading Multinational Medical Device organisation in the Cork area is looking for a Regulatory Affairs Specialist II to join their growing team. This is an opportunity to work in an award-winning and innovative company.
The ideal candidate will have:
-Previous experience with technical documents
-Experience working with international groups in areas such as the EU, USA, Japan
-Knowledge of MDR changes
-Experience in MDD, FDA, ISO environment
-Strong communications and influencing skills
What you will be doing: (Full job spec available on request)
–Review and approve documentation related to product release
-Providing updates on regulatory requirement changes.
-Provide input, review and approve facility regulatory activities such as labelling
For a confidential discussion and more information on the role, please contact Aisling on 021 4809118 or email email@example.com