Opportunity Description
Responsibilities:
Responsible for representing QA on cross-functional teams and executing Quality System requirements to ensure products are properly transferred from development to manufacturing and maintained on market.
Responsible for assuring compliance to local, divisional, and corporate policies and external agency regulations worldwide.
Products include medical devices and combination products, such as infusion pumps, enteral and sub-cutaneous tubing, Pre-filled Syringes, Autoinjectors, Eyecare Products, Aesthetics Devices, etc.
Primary driver for the quality and compliance aspects of Design transfer and on-market change management.
Serve as the primary quality lead for design transfer activities to enable product launch, including transfers both within and outside of client.
Mentor/lead product team members through the design transfer process providing guidance to assure optimal approach. <...
Full-time
Engineers