Viridian Therapeutics, Inc.

Associate Director, Medical Device Quality Join to apply for the Associate Director, Medical Device Quality role at Viridian Therapeutics, Inc. About the Role Reporting to the Sr. Director, Medical Device Quality, the Associate Director is responsible for providing leadership and compliance oversight of quality activities associated with medical devices and combination product development that meet applicable regulatory requirements and industry standards. The role supports the development and manufacturing of combination products at contract manufacturing organizations (CMOs) and is based in our Waltham, MA headquarters. Office‑based employees are required to work in the office three (3) days a week. Responsibilities Represent medical device quality as subject matter expert and core team member on device development projects. Support design and development phases, clinical readiness, commercial approval/launch, and regulatory submissions of Viridian combination product...

Description At Viridian, we are focused on developing best-in-class medicines for people living with autoimmune and rare diseases. Leveraging our team's expertise in antibody discovery and engineering, we have created a robust pipeline of differentiated investigational therapeutic candidates for well-validated targets. Reporting to the Sr. Director, Medical Device Quality, the Associate Director is responsible for providing leadership and compliance oversight of quality activities associated with medical devices and combination product development that meet applicable regulatory requirements and industry standards. The Associate Director will play a critical role in development and manufacturing of combination products at contract manufacturing organizations (CMOs). This role is based in our Waltham, MA headquarters. Our office-based employees are required to work in the office three (3) days a week. Responsibilities (including, but not limited to): • Represent medical...