The position is primarily responsible for design/review of product labels, prepare labels to be included in regulatory submissions, and management of FDA GUDID, EU Eudamed and device approval databases. Additional responsibilities include software validations, supporting regulatory submissions/certifications outside the United States, and internal audits. It requires both attention to detail and process. This position reports directly to the Company's Senior Director of Regulatory Affairs and Quality Assurance. Requirements   A bachelor's degree in a scientific or technical discipline with 1-3 years of relevant industry experience in quality or regulatory affairs; Self-motivated, self-directing, strong attention to detail; excellent organizational and time management skills; Excellent computer skills Strong interpersonal and project management skills with the ability to communicate well, verbally and in writing; Multi-lingual skills are beneficial; RAC...