Regulatory Affairs Specialist, Medical Devices - Rochester

A leading technology manufacturer in Rochester, MN, seeks a Regulatory Affairs Specialist to perform compliance reviews and audits of regulatory documentation for manufacturing processes. This role requires strong expertise in ISO 13485 and FDA regulations, alongside a collaborative approach in engaging with key customers. Ideal candidates will have over 5 years of regulatory experience, excellent problem-solving skills, and the ability to contribute to continuous improvement initiatives. A 4-year degree is required, along with effective communication skills. #J-18808-Ljbffr