ABBOTT LABORATORIES Regulatory Affairs Project Coordinator Salary in the United States

At Abbott, diverse ideas, perspectives, and expertise allow us to create the life-changing solutions that help people live healthier lives. In 150 countries and with businesses spanning nutrition, diagnostics, medical devices, and branded generic pharmaceuticals, Abbott offers you enormous opportunities to explore your interests and help you achieve your career and personal goals.

Abbott Rapid Diagnostics is part of Abbott’s Diagnostics family of businesses, bringing together exceptional teams of experts and industry leading technologies to support diagnostic testing which provides important information for treatment and management of diseases and other conditions.

The position is within our Abbott Rapid Diagnostics. This person will work with project managers and teams to manage the project lifecycle for company's products and services involving functional teams focused on the delivery of new or existing products. This job description will be reviewed periodically and is subject to change by management.

• Independently identifies opportunities to improve the efficiency and effectiveness of the project management systems and process being examined, including integrating internal and external best practices and benchmarking data

• Supports project execution which may include identifying tasks, tracking project schedule, and identify/manage risks and issues, and independently executing assigned tasks.

• Begins establishing and cultivating a network of internal resources to facilitate completion of tasks.

• Participates in special projects as they arise.

• Provides Divisional support as it relates to project management tools and software.

• Manage day-to-day regulatory reporting on new and existing products.

• May exercise authority within pre-established limits and approval.

• Independently manages own work load by balancing multiple tasks/projects, prioritizing work based on criticality and urgency, and completing tasks on time.

• Bachelor's degree

• 3-5 years of related regulatory work experience within medical device or pharmaceutical industries