Senior Global Regulatory Projects Manager, Medical Devices

Regulatory Jobs; Santa Clara (CA); Presencial; USD 90.000 - 180.000; Tempo integral

Benefícios oferecidos por esta vaga

Health insurance

Retirement plan with employer matching

Tuition reimbursement

Education benefit – FreeU

Resumo da vaga

Abbott is a global healthcare leader delivering life-changing technologies across diagnostics, devices, and nutrition. This Senior Regulatory Project Management Specialist role coordinates complex regulatory initiatives in global markets, collaborating with Regulatory Affairs, R&D, Quality, and Operations to ensure timely submissions and registrations.

You will plan, monitor, and report on milestones, navigate cross-geo teams, and drive alignment to accelerate product approvals while ensuring

Qualificações

• Bachelor’s degree required.
• Minimum 5 years of project management experience.
• Experience in regulatory, quality, or product management in medical devices preferred.

Responsabilidades

• Lead planning, coordination, and execution of global regulatory projects for product registrations and lifecycle management.
• Develop detailed project plans, timelines, milestones, and tracking tools.
• Coordinate with Regulatory Affairs, R&D, Quality, Clinical, Operations, and other teams.
• Monitor progress, identify risks, issues, and resource constraints; implement mitigation plans.
• Facilitate cross-functional meetings; assign ownership and drive accountability.
• Communicate project status and metrics to stakeholders and leadership regularly.
• Support multiple concurrent projects across geographies, balancing priorities.
• Coordinate inputs to support budget cycles and project decisions.

Conhecimentos

Project management

Cross-functional collaboration

Formação

Bachelor’s degree

Descrição da vaga

Abbott is a global healthcare leader delivering life-changing technologies across diagnostics, devices, and nutrition. This Senior Regulatory Project Management Specialist role coordinates complex regulatory initiatives in global markets, collaborating with Regulatory Affairs, R&D, Quality, and Operations to ensure timely submissions and registrations.

You will plan, monitor, and report on milestones, navigate cross-geo teams, and drive alignment to accelerate product approvals while ensuring