We anticipate the application window for this opening will close on - 17 Sep 2025
At Medtronic you can begin a life-long career of exploration and innovation, while helping champion healthcare access and equity for all. You’ll lead with purpose, breaking down barriers to innovation in a more connected, compassionate world.

REQUIRED QUALIFICATIONS:

Requires advanced knowledge of job area combining breadth and depth, typically obtained through advanced education combined with experience.
May have practical knowledge of project management.
Requires 4+ years of experience with a with a High School Diploma or equivalent or Advanced Degree with a minimum of 2 years relevant experience.

PHYSICAL JOB REQUIREMENTS

The above statements are intended to describe the general nature and level of work being performed by employees assigned to this position, but they are not an exhaustive list of all the required responsibilities and skills of this position.
The physical demands described within the Responsibilities section of this job description are representative of those that must be met by an employee to successfully perform the essential functions of this job. Reasonable accommodations may be made to enable individuals with disabilities to perform the essential functions. For Office Roles: While performing the duties of this job, the employee is regularly required to be independently mobile. The employee is also required to interact with a computer, and communicate with peers and co-workers. Contact your manager or local HR to understand the Work Conditions and Physical requirements that may be specific to each role.

• Maintain and support the company’s electronic quality management system (eQMS).
• Monitor and analyze quality system metrics, identifying trends and opportunities for improvement.
• Assist with the management of quality system processes, including CAPA, complaints, nonconformances, internal audits, training, and document control.
• Generate reports and dashboards to support compliance monitoring and management reviews.
• Ensure timely and compliant documentation and record-keeping in accordance with FDA and ISO requirements.
• Participate in internal and external audits, providing data and system support.
• Collaborate with cross-functional teams to support quality initiatives and continuous improvement projects.
• Support change management and system updates to maintain compliance and usability