Senior MDR Vigilance Supervisor

Welcome to Medtronic! We are a global leader in medical technology, providing life-saving and life-changing solutions to patients around the world. We are currently seeking a highly skilled and experienced Senior MDR Vigilance Supervisor to join our team.As the Senior MDR Vigilance Supervisor, you will play a crucial role in ensuring compliance with Medical Device Regulation (MDR) requirements and driving our vigilance process. Your expertise and leadership will be vital in identifying, evaluating, and reporting adverse events related to our medical devices, ultimately contributing to our mission of improving patient outcomes.To excel in this role, you must have a strong understanding of MDR regulations and experience in managing vigilance activities within the medical device industry. You should also possess excellent communication, problem-solving, and project management skills.If you are looking for a challenging and rewarding opportunity to make a difference in the lives of patients and work with a dynamic and passionate team, we encourage you to apply for the Senior MDR Vigilance Supervisor position at Medtronic.

1. Oversee and manage the entire vigilance process for medical devices, ensuring compliance with MDR requirements.
2. Develop and maintain a comprehensive understanding of MDR regulations and guidelines.
3. Lead and mentor a team of MDR vigilance professionals, providing guidance and support as needed.
4. Identify, evaluate, and report adverse events related to Medtronic medical devices.
5. Collaborate with cross-functional teams to investigate and resolve any quality or safety issues that arise.
6. Develop and implement strategies to improve the vigilance process and ensure timely reporting of adverse events.
7. Review and analyze data to identify trends and potential risks, and make recommendations for corrective actions.
8. Serve as a subject matter expert on MDR regulations and requirements, providing guidance and training to other departments as needed.
9. Communicate with regulatory agencies regarding adverse event reporting and other vigilance-related matters.
10. Work closely with product development teams to ensure MDR compliance during the design and development process.
11. Prepare and submit reports to regulatory agencies as required by MDR regulations.
12. Stay up-to-date with changes and updates to MDR regulations and incorporate them into the vigilance process as necessary.
13. Participate in internal and external audits to ensure compliance with MDR regulations and company policies.
14. Foster a culture of safety and continuous improvement within the vigilance team and throughout the organization.
15. Represent Medtronic at industry conferences and events, sharing knowledge and best practices related to MDR vigilance.

According to JobzMall, the average salary range for a Senior MDR Vigilance Supervisor in Minneapolis, MN, USA is between $80,000 and $110,000 per year. This range can vary depending on factors such as experience, qualifications, and the specific company or organization the supervisor is working for. Other factors that can affect salary include the industry and the size of the company. Generally, larger companies or those in industries with higher demand for this role may offer higher salaries. Additionally, experience and advanced degrees or certifications in this field may also lead to higher pay.

Medtronic plc is the world's largest medical device company that generates the majority of its sales and profits from the US healthcare system and is headquartered on the island of Ireland.