BP Program Manager - LP

Job description

We anticipate the application window for this opening will close on - 2 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 LifeAs part of the Strategy and Technology Group, the Program Management Office (PMO) enables the successful execution of Enterprise Operations strategy through innovative program management solutions and technical expertise. By leading transformational initiatives and aligning cross-functional teams, we drive operational excellence and create enterprise-wide impact. As trusted partners, we cultivate collaboration across Medtronic to deliver the One Best Way. The BP Program Manager will lead and coordinate Warsaw site activities across multiple strategic programs and projects. This role is responsible for driving execution excellence by managing project interdependencies, mitigating risks, coordinating site priorities, and ensuring alignment across cross-functional teams. The position serves as a key liaison between site leadership, functional teams, and the PMO organization, ensuring projects are delivered on schedule, within budget, and in compliance with quality and regulatory requirements. The successful candidate will drive measurable business and operational outcomes while fostering collaboration and accountability across stakeholders. This role will be based onsite 4+ days/week at our Warsaw facility Provide site-level portfolio coordination, balance project priorities across multiple strategic initiatives, and ensure optimal resource utilization to achieve business objectives Lead and manage all phases of program and project execution, including feasibility, planning, execution, monitoring, and closure, in accordance with PMO governance standards and business processes Direct site-level project execution for multiple concurrent initiatives, ensuring alignment with strategic objectives and operational priorities Identify, assess, and manage project interdependencies, risks, issues, and resource constraints to enable successful execution Serve as the primary interface between project teams, site leadership, functional departments, and PMO stakeholders Lead cross-functional teams to achieve project milestones while ensuring adherence to scope, schedule, budget, and quality objectives Develop and maintain integrated project plans, resource forecasts, risk mitigation strategies, and executive-level status reporting Review project performance metrics and financials, proactively addressing variances and implementing corrective actions when required Manage end-to-end project execution, including manufacturing facility readiness, equipment and line qualification, process implementation, technology transfer, and operational deployment activities Drive effective decision-making through structured problem solving, data analysis, and stakeholder engagement Establish monitoring and governance mechanisms to track progress, escalate risks, and support timely issue resolution Promote a culture of accountability, collaboration, continuous improvement, and operational excellence across project teams Minimal travel as needed Required Qualifications Bachelor’s Degree and 5+ years of experience OR advanced degree and 3+ years of experience Experience leading projects, programs, and/or teams Experience working within regulated industries, preferably medical devices, or similarly regulated environments Preferred Qualifications Degree in Industrial engineering, Mechanical Engineering, Materials Science, Chemical Engineering, Manufacturing Engineering, or a related technical discipline. Experience in Engineering, Manufacturing, Product Development, Operations, or Technical Program Management Demonstrated success leading complex, cross-functional programs involving multiple stakeholders and competing priorities Strong understanding of project management methodologies, governance frameworks, and portfolio execution principles Experience supporting medical device product development, commercialization, sustaining engineering, or manufacturing operations Working knowledge of Design Controls, FDA Quality System Regulations, ISO 13485, and related regulatory requirements. Experience with manufacturing automation, advanced manufacturing engineering, process development, equipment qualification, and validation Proven track record leading technology transfers, process scale-up initiatives, manufacturing readiness activities, and site implementation projects PMP, Agile, Lean Six Sigma, or equivalent project management/process improvement certification 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 contributions. They share in the success they help to create. We offer a wide range of benefits, resources, and competitive compensation plans designed to support you at every career and life stage. Salary ranges for U.S (excl. PR) locations (USD):$120,000.00 - $180,000.00 This position is eligible for a short-term incentive called the Med