Medical Device Regulatory Specialist


Job ID: 130627 Industry: CLINICAL


Regulatory Affairs Specialist


Our client is a large medical device company that focuses on class III medical devices. Right now they are looking for someone to come on board to support their fulltime staff as they have someone going on maternity leave. This person will be focusing on cardiac devices and PMA submissions.



The project will entail a series of PMA submissions around cardiac devices. The majority of the work will be supporting fulltime day to day efforts and not project focused. This person must be a subject matter expert in PMA submissions for class III medical devices. They will be responsible for the hands on writing of the submissions and providing guidance to other fulltime employees on how to effectively submit a PMA. The client is working with cardiac devices so any experience with submitting class III cardiac devices is preferred.



Regulatory Affairs Specialist


Medical Devices

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