Associate Director Plasma - Lexington, MA
1 month ago
The role drives collaboration with internal and external partners, on all life cycle management efforts (e.g. post market surveillance, risk management, change requests, etc.).
AD PVDQ ensures that Takeda's medical devices and combination products stay in compliance with global regulatory requirements and international standards (e.g., ISO, AAMI, ANSI).
This role actively identifies, leads, and drives implementation of Continuous Improvement (CI) projects in line with department goals, key business outcomes,Job summary
- Provides industry-leading quality leadership and support for quality life cycle management activities
Job description
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