Post Market Regulatory Affairs Specialist

Responsible for supporting Post Market Regulatory Affairs activities associated with complaint handling and MDR submissions. Collaborates with Quality, Engineering, Manufacturing, Product Development and other functional experts. Interacts with internal and external business partners and colleagues.

Requirements

• Ability to work in a cross-functional matrix environment
• Strong verbal and written communication skills
• Proficiency in MS Office (Word, Excel, Outlook, PowerPoint, Sharepoint)
• Knowledge of basic medical terminology
• 2-4 years of related work experience