Manager, Regulatory Affairs And Compliance (Tecate)

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 An experienced individual to provide hands‐on leadership for the Manufacturing (D&D) team, who will champion the Nordson MEDICAL New Product Introduction (NPI) Process.