PD Program Manager - NMPH - Rice Creek/Fridley, MN (Onsite)

Job description

We anticipate the application window for this opening will close on - 7 Sep 2026 Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year. Your unique talents will help shape the future of healthcare while building a career grounded in purpose, growth, and impact. A Day in the LifeAcross our global Neuroscience organization, we develop innovative therapies for complex neurological, spinal, and pelvic health conditions. Our Neuromodulation team delivers advanced solutions for chronic pain and movement disorders through spinal cord stimulation, deep brain stimulation, and targeted drug delivery systems. Our Pelvic Health team advances minimally invasive neuromodulation therapies for bladder and bowel control conditions, helping patients regain function and improve quality of life. Located at Medtronic's location in Rice Creek/Fridley, MN, this role is onsite four days per week and requires <10% travel. Check us out on LinkedIn: Medtronic Brain Modulation and Pain Interventions Check us out on LinkedIn: Medtronic Pelvic Health As a PD Program Manager, you will lead complex, cross-functional programs within the Neuromodulation (NM) and Pelvic Health (PH) Product Lifecycle Management organization. In this role, you will drive strategic initiatives across the released product portfolio, including regulatory compliance remediation (such as MDR), manufacturing capacity expansion, product design enhancements, supply continuity efforts, and other business-critical programs that support patients and healthcare providers worldwide. You will work with a diverse portfolio of technologies, including implantable and external neurostimulators, implantable infusion pumps, leads, catheters, software programming applications, and device recharge and programming systems. Success in this role requires strong leadership, collaboration, and execution skills. You will partner with cross-functional stakeholders across R&D, Regulatory Affairs, Quality, Operations, Supply Chain, Manufacturing, Biocompatibility, Sterilization, and other functions to align priorities, manage risks, and deliver program objectives. The ideal candidate has a proven track record of leading complex, multi-site programs in a highly matrixed environment and combines technical expertise, business acumen, and program management excellence with a strong understanding of medical device development and operations. Responsibilities may include the following and other duties may be assigned: Develop and maintain project plans, schedules, and resource allocation for assigned programs, ensuring alignment with business strategies and applicable medical device regulations. Facilitate effective communication among stakeholders, providing regular updates on project progress and strategic impact Manage technical risks and issues by working with the technical team to develop and maintain risk burndown plans Reviews status of projects and budgets; manages schedules and prepares status reports. Assesses project issues and develops resolutions to meet productivity, quality, and client-satisfaction goals and objectives. Develops mechanisms for monitoring project progress and for intervention and problem solving. Gathers requirements, works on requirements planning, requirements elicitation and requirements management to ensure they meet demands of project’s key stakeholders. Communicates with stakeholders, obtains stakeholder engagement to ensure the end products or processes will solve the business problems. Minimum Requirements (Must Haves): Bachelor's degree in Engineering or Technical field with minimum of 5 years of relevant experience, OR, Advance degree in Business, Engineering or Technical field with minimum of 3 years of relevant experience Nice to Have: MBA or advanced degree preferred. 3+ years of experience leading projects, programs, and/or people in a cross-functional environment. Lean Six Sigma Black Belt, PMP, or other project management certifications preferred. Experience leading complex regulatory compliance initiatives, including MDR remediation programs. Demonstrated experience in the design, development, and/or manufacturing of medical devices. Working knowledge of regulatory submissions and global regulatory requirements, including FDA 510(k) and PMA processes. Experience operating within Quality Management Systems (QMS), with a strong understanding of Design History Files (DHF), Device Master Records (DMR), and design control requirements. Knowledge of applicable medical device standards and regulations, including IEC 60601, IEC 62304, ISO 14971, and ISO 13485. Strong critical thinking, analytical, and problem-solving skills, with the ability to navigate complex technical and business challenges. Ability to interpret technical data, engineering reports, and statistical analyses to support informed decision-making. Proven ability to influence and collaborate effectively across a highly matrixed organization and drive results through cross-functional teams. For Baccalaureate degrees earned outside of the United States, a degree that satisfies the requirements of 8 C.F.R. § 214.2(h)(4)(iii)(A) is required. 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. U.S. Work Authorization & Sponsorship At Medtronic, we are committed to fostering an environment where employees can thrive and make a meaningful impact. In alignment with our enterprise-wide workforce planning approach, U.S. work authorization sponsorship (H-1B, TN, J, etc.) is offered exclusively for Principal-level roles and above, where specialized expertise aligns with long-term business needs. Roles below the Principal level require candidates to possess unrestricted U.S. work authorization at the time of hire and for the duration of employment. ‌ Recruitment Fraud Alert We are aware of phishing scams targeting job seekers. Please keep the following in mind: Apply only through official Medtronic channels. All legitimate Medtronic recruiting communications come from approved Medtronic platforms and official @medtronic.com email addresses. Medtronic will never ask for payment or sensitive personal information (such as bank account or Social Security details) during early stages of the hiring process. Any such requests are not legitimate. If you receive a suspicious message claiming to be from Medtronic, do not respond, click links, or open attachments. If you have any questions, concerns regarding the authenticity of a communication alleged to have been made by or on behalf of Medtronic, please contact us immediately at AskHR@medtronic.com. ‌ Benefits & Compensation Medtronic offers a competitive Salary and flexible Benefits Package A commitment to our employees lives at the core of our values. We recognize their contr