MDR / Vigilance Manager

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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