Senior Regulatory Specialist Role
This role offers a challenging opportunity to work in the implementation of post-market activities within a rapidly growing medical device company.
* The successful candidate will play a key part in the development and execution of regulatory strategies.
* Responsibilities include approval of Vigilance/MDR reporting, support for Regulatory Post Market System improvements, participation in Field Safety Corrective Action planning and associated tasks as required.
Requirements:
* A degree level qualification in Engineering, Science, QA, or related field is essential.
* A minimum of five years experience at a senior regulatory level in the medical device industry is crucial.