Global Regulatory Projects Lead — Medical Devices

Abbott; Santa Clara (CA); On-site; USD 90,000 - 180,000; Full time

Benefits offered by this job

Career development

HIP PPO medical plan

Retirement plan with high employer<br>

Tuition reimbursement

FreeU education benefit

Job summary

Abbott in Santa Clara, CA, is seeking a Senior Regulatory Project Management Specialist to drive global regulatory initiatives for its medical device portfolio. You will coordinate cross-functional teams, manage regulatory submissions across international markets, and ensure on-time delivery of milestones in a fast-paced environment.

We value strong project management, stakeholder engagement, and the ability to navigate complex regulatory landscapes to enable growth and patient access worldwide.

Qualifications

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

Responsibilities

• Lead the planning, coordination, and execution of global regulatory projects for product registrations, submissions, and lifecycle management across international markets.
• Develop and maintain detailed project plans, timelines, milestones, and tracking tools to ensure timely delivery.
• Coordinate with Regulatory Affairs, R&D, Quality, Clinical, Operations, and other teams to ensure project success.

Skills

Project management

Regulatory affairs

Cross-functional collaboration

Stakeholder communication

Education

Bachelor’s degree

Job description

Abbott in Santa Clara, CA, is seeking a Senior Regulatory Project Management Specialist to drive global regulatory initiatives for its medical device portfolio. You will coordinate cross-functional teams, manage regulatory submissions across international markets, and ensure on-time delivery of milestones in a fast-paced environment.

We value strong project management, stakeholder engagement, and the ability to navigate complex regulatory landscapes to enable growth and patient access worldwide.