Global Medical Device Regulatory Affairs Associate

A global medical technology company located in the Town of Poland seeks a Regulatory Affairs Specialist to conduct regulatory assessments, manage licenses, and prepare FDA submissions. The ideal candidate holds a Bachelor's degree and has a minimum of 4 years of experience in Regulatory Affairs within the medical device sector. Strong communication and problem-solving skills, along with fluency in English, are essential for success in this role. #J-18808-Ljbffr