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- Bachelor's, or higher, degree in science/technology program preferred
- 5+ years of experience in a cGMP Quality Assurance/Compliant environment (medical devices preferred)
- The Senior Quality Analyst is responsible for assuring that activities, processes, and product related to managing the processes of CAPA, Change Management, investigations, deviations, Quality Management Review, Audit coordination, and metrics for the Madison facility This position will have a wide range of tasks which may include Quality System improvement initiatives, data maintenance, trending and reporting, deviation investigation, internal/external auditing, and direct involvement and collaboration with the Regulatory Affairs, Operations, Technical Operations, Engineering, and Materials Management groups to drive quality culture.
Date Posted: 28 April 2025
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