We anticipate the application window for this opening will close on - 6 Oct 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.

A Day in the Life

The Senior PD Project Management Specialist in RS&C is responsible for leading complex, cross-functional product projects from concept through commercialization. This role blends advanced project management expertise with deep knowledge of product development processes, ensuring projects are executed efficiently, on time, within budget, and in compliance with regulatory standards. The incumbent will drive project strategy, resource management, and risk mitigation while fostering a collaborative environment across multiple teams within RS&C (RA, RO, TC).

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.

Responsibilities may include the following and other duties may be assigned.

• Lead and manage RS&C teams through all phases of the product development lifecycle, from feasibility and design to validation, launch, and post-market support. 

• Develop and maintain comprehensive project plans, including timelines, budgets, deliverables, and resource allocation. 

• Collaborate with R&D, Regulatory, Quality, Marketing, Clinical, Manufacturing, and other stakeholders to ensure alignment and achievement of project objectives in respect to Global Regulatory and Labeling strategy and implementation. 

• Identify, assess, and proactively manage project risks; develop and implement mitigation strategies. 

• Prepare and deliver regular project updates, status reports, and presentations to senior leadership and other stakeholders. 

• Ensure compliance with internal and external regulatory requirements (e.g., FDA, ISO) throughout the project. 

• Drive continuous process improvement initiatives to enhance project execution and product quality. 

• Mentor and coach junior project managers and team members on best practices in project and product development management. 

• Support the development and implementation of project management tools, methodologies, and standard work. 

• Lead or participate in business process improvement efforts related to product development and project delivery. 

Must Have: Minimum Requirements

• Bachelor’s degree required and 4 years of relevant experience
• Or, advanced degree and 2 years of relevant experience

Nice To Have

• project management experience, with at least 3 years in product development within a regulated industry (medical device, pharmaceutical, etc.). 

• Demonstrated success managing complex, cross-functional projects from concept to commercialization. 

• Strong knowledge of product development processes, design controls, and regulatory requirements. 

• Experience with resource management, budget oversight, and risk management. 

• Proficiency in project management software and tools. 

• Outstanding organizational, leadership, and communication skills. 

• PMP or equivalent project management certification preferred.