The SENIOR REGULATORY AFFAIRS SPECIALIST will provide Regulatory Affairs expertise, participate in the day-to-day operations of the department and be responsible for preparing and managing technical files and regulatory submissions for implantable STRUCTURAL HEART devices in compliance with medical device regulations in the US, EU (MDD/MDR) and other parts of the world.
JOB DESCRIPTION: The Senior Staff Engineer owns embedded system development from requirements through commercial launch while providing influence and contributing...Apply For This Job
Position Overview The primary role of the Therapy Manager is to provide first class clinical training and education to current...Apply For This Job
The Senior Financial Analyst is Responsible for supporting the CRM R&D and Marketing teams meet their Financial & Operational targets by performing the financial close process, budgeting process, balance...Apply For This Job
Virtual Reality Program Lead Are you interested in new technology such as Virtual Reality? Have you ever worked in a clinical setting...Apply For This Job
Key Responsibilities: Leads development and authoring of program-level and study-specific regulatory documents, including protocols, protocol amendments, Investigator’s Brochures, clinical study...Apply For This Job