MDR / Vigilance Manager
This job is no longer available.
A Day in the Life
- § You will identify and lead department initiatives that result in the resolution of CVG PXM opportunities to increase operational efficiency, quality, consistency, compliance and cost effectiveness
- § You will support the preparation of CVG reports and analytical tools that will be used for internal decision making, potential reporting to regulatory agencies, and fulfilling business partner queries
- § You will provide direction for the complaint registration process
- § You will lead preventative and corrective action activities
- § You will represent the complaint handling process to external regulators and internal auditors
- § You will serve as the manager of the team and actively contribute to talent acquisition and talent management for the department
- § You will participate in the Annual Operating Plan and develop and administer budgets, schedules and performance standards
Must Have: Minimum Requirements
You will have a Bachelor’s degree and 5+ years’ experience in the medical device industry.
Nice to Have
- § Bachelor’s degree in healthcare, engineering or bioscience field
- § Experience managing or supervising a team
- § Experience managing and leading FDA inspections and responses
- § Experience leading complaint teams and adverse event reporting
§ Knowledge of CVG products
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