Sr Ethics and Compliance Program Manager - Diabetes
Listed on 2026-02-09
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Healthcare
Healthcare Management
We anticipate the application window for this opening will close on February 7, 2026.
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.
A Day in the LifeWe are seeking a strategic, experienced, and proactive Ethics and Compliance Program Manager to help design and build the global compliance program for Medtronic Diabetes – a $2.8 billion medical device business that has recently announced that it will be spinning out into a standalone public company. Reporting to the company’s Chief Compliance Officer, the Compliance Program Manager will play a pivotal role in helping the company prepare for and operate successfully as a publicly traded company, aligning compliance programs with public company standards and shareholder expectations.
In this role, you will support the execution of key operational initiatives that enhance the effectiveness, efficiency, and scalability of the compliance function.
This position is an exciting opportunity to work with Medtronic s Diabetes business. Medtronic has announced its intention to separate the Diabetes division to promote future growth and innovation within the business and reallocate investments and resources across Medtronic, subject to applicable information and consultation requirements. This separation provides our team with a bold opportunity to unleash our potential, enabling us to operate with greater speed and agility.
As a separate entity, we anticipate leveraging increased investments to drive meaningful innovation and enhance our impact on patient care.
This role requires you to work on-site at least 3 days per week at one of locations in:
- Northridge, CA
- Minneapolis, MN
- San Antonio, TX
- Serve as a critical member of the compliance team and support the development and implementation of the global compliance program to effectively mitigate compliance risks associated with the sale of diabetes products to HCP interactions and directly to patients.
- Provide strategic oversight and direction for major elements of the global compliance program, such as the policy, training and/or auditing and monitoring programs and support other elements of the compliance program, as needed.
- Lead initiatives that enhance global program maturity, ensuring alignment with regulatory requirements, industry best practices, and evolving business models.
- Support the hotline and investigation program and conduct certain investigations.
- Influence long-term compliance strategy through participation in the risk assessment process and the development of the compliance strategic workplan.
- Advise the business on matters involving HCP Interactions and manage HCP interactions compliance-related reviews and processes, including transparency reporting.
- Oversee high-impact compliance initiatives and facilitate change management, including milestone tracking, stakeholder engagement, communication planning, training deployment, and executive reporting.
- Guide complex compliance reviews, approvals, and risk-based decision-making.
- Develop actionable metrics and leverage insights to identify trends, emerging risks, and opportunities to elevate program effectiveness.
- Drive operational efficiency by optimizing workflows, identifying bottlenecks, and simplifying processes while effectively managing risk.
- Lead projects that modernize compliance operations, including technology enablement, automation, and the adoption of artificial intelligence to streamline monitoring, approvals, and risk management activities.
Required Qualifications
- Bachelor s degree and 7 years of relevant experience
- Or, advanced degree and 5 years of relevant experience
- Juris Doctor (JD) degree
- 7 years of experience in senior compliance roles, ideally within a publicly traded medical device, biotech, or pharmaceutical company.
- Deep knowledge of medical device regulatory environments (e.g., AKS, FCA, Transparency laws) and the DOJ and OIG compliance program guidance documents.
- Familiarity with…
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