Regulatory V&V Specialist — Medical Devices

A medical device company in Jacksonville, FL is seeking a Regulatory V&V Specialist to assist with verification and validation activities for products in development. The role requires a BS degree in a scientific discipline and 2-4 years of experience in the Medical Device Industry, specifically with biocompatibility and ISO 10993 compliance. The individual will collaborate with cross-functional teams to ensure regulatory submissions meet the requirements, maintain documentation, and support the overall product development lifecycle. Competitive benefits and in-house training are offered. #J-18808-Ljbffr