Manager, Regulatory Affairs and Compliance

Job Summary

A high-performing individual to provide hands-on leadership to the Finished Device Solutions (D&D) team, and to be a key individual in the areas of Quality Management. Medical device development and manufacture experience is essential. Injection molding experience is also a strong plus. The individual will possess a broad range of medical device quality skills and experience, a record of leading and participating with teams from product concept through validation and into manufacturing, as well as in-depth knowledge in several clinical and product areas. This individual will also play a key role in mentoring less experienced employees and must be self-motivated and excited by the prospect of working in a dynamic, entrepreneurial environment.

Essential Job Duties and Responsibilities

Qualifications