Description: Work Flexibility: Onsite What You Will Do: Technical Responsibilities: Under minimal supervision, research, design, develop, modify, and verify components/modules for medical device product development and/or misc. activities.Translate and/or ...
27 days ago
... and supporting GxP systems, including clinical, regulatory, and quality applicationsHands-on ...
7 days ago
... manage and support enterprise R&D applications (Clinical, Regulatory, Quality). Responsible for configuration ...
7 days ago