Job Details

A leading medical device company is seeking a Regulatory Affairs Specialist to develop and execute strategies for medical devices, including wearable technology. The role requires 8-10 years of experience in US and EU regulatory affairs and strong project management skills. You will lead FDA submissions and interact with regulatory authorities to ensure compliance. This full-time position offers a competitive salary and excellent benefits, including medical, dental, and a 401(K) plan.#J-18808-Ljbffr