Senior Regulatory Project Management Specialist (on-site)

At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You’ll also have access to:

• Career development with an international company where you can grow the career you dream of.
• Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.
• An excellent retirement savings plan with a high employer contribution.
• Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor’s degree.
• A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.
• A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.

• Lead the planning, coordination, and execution of global regulatory projects supporting product registrations, submissions, approvals, and lifecycle management activities across international markets.
• Develop and maintain detailed project plans, timelines, milestones, and tracking tools to ensure project deliverables are completed on schedule and aligned with business priorities.
• Partner closely with Regulatory Affairs, R&D, Quality, Clinical, Operations, and other functional teams to coordinate activities and ensure successful project execution.
• Monitor project progress, identify risks, issues, and resource constraints, and drive mitigation plans to minimize delays and maintain project momentum.
• Facilitate cross-functional meetings, establish action plans, assign clear ownership, and follow through on key deliverables to ensure accountability and execution.
• Track and communicate project status, critical path activities, key decisions, and metrics to stakeholders and leadership through regular reporting and project reviews.
• Support multiple concurrent projects across various geographies, balancing competing priorities while maintaining a strong focus on execution and results.
• Coordinate inputs to support financial budget cycle activities and project decisions

• Bachelor’s degree.
• Minimum 5 years of project management or related experience.

• 6+ years relevant experience in regulatory, quality, or product management in medical device industry.
• Experience with OUS / International medical device product registrations.
• Demonstrated ability to manage all aspects of large-scale, complex projects from start to finish.
• Experience developing project plans, schedules, budgets, forecasts, and resource plans.
• Ability to coordinate cross-functional resources and manage project execution to achieve objectives.
• Experience conducting project meetings, tracking progress, and communicating project status through reports and stakeholder updates.
• Ability to manage meetings across global time zones on a regular basis.

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In specific locations, the pay range may vary from the range posted.