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Ethics and Compliance Program Manager - Diabetes
MedtronicNorthridge, United Statesfull_timeVerifiedPosted 20 Jan 2026
💰 $166,800/yr
About the role
We anticipate the application window for this opening will close on - 26 Jan 2026
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
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 Life
We are seeking a strategic, experienced, and proactive 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
Responsibilities may include the following and other duties may be assigned.
- 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.
- Manage element(s) of the compliance program, such as the policy, training and/or auditing and monitoring programs and support other elements of the compliance program, as needed.
- Manage the hotline and investigation program, including collaborating with legal, human resources and other cross-functional and local resources, as appropriate, to conduct investigations.
- Participate 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 and escalate issues to compliance leadership, as needed.
- Develop actionable metrics and leverage insights to identify trends, emerging risks, and opportunities to elevate program effectiveness
- Project manage key compliance initiatives, tracking milestones, documentation, training, and reporting deliverables
- Drive operational efficiency by optimizing workflows, identifying bottlenecks, and simplifying processes while effectively managing risk
- Utilize technology, including artificial intelligence, to streamline compliance process and effectively manage risk.
Required Qualifications:
- Bachelor's degree and 5 years of relevant experience
- Or, advanced degree and 3 years of relevant experience
Preferred Qualifications:
Juris Doctor (JD) degree
- 5 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 Anti-Bribery, anti-corruption, anti- trust and competition laws.
- Experience with compliance-related technologies (e.g., third-party screening, transparency and Sunshine Act reporting platforms, HCP interaction platforms, etc.) and other workflow and automation technologies.
- Project management skills and familiarity with operational efficiencies or continuous improvement methodologies (e.g. Lean, Six Sigma)
- Experience managing compliance in a multinational environment.
- Proven leadership and a track record of building high performing teams.
- Excellent interpersonal, communication, and presentation skills.
- Demonstrated ability to work with senior leadership
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