Associate Director, Medical Affairs Quality Assurance - Remote

Overview

AbbVie is dedicated to delivering a consistent stream of innovative, safe, and effective quality medicines and products that solve serious health issues and have a remarkable impact on people’s lives. The Associate Director, Safety, Medical & Regulatory Quality is part of the R&D Quality Medical Affairs QA team which provides independent quality oversight of AbbVie’s Medical Affairs and Health Impact function.

In Short

• Contribute to continuous compliance with global regulations.
• Develop and execute a holistic quality assurance model.
• Demonstrate AbbVie’s Ways of Working and Leadership Attributes.
• Lead innovative quality strategies and solutions.
• Evaluate risks impacting compliance and propose mitigations.
• Support business process owners to ensure quality integration.
• Participate in Regulatory Authority inspection activities.
• Consult on worldwide regulations and corporate policies.
• Analyze and report metrics for compliance status.
• Drive change and efficiency through feedback and recommendations.

Requirements

• Bachelor's degree in Biology, Nursing, Pharmacy, or related field.
• 5 years of experience in Medical Affairs or Quality Assurance.
• Strong analytical and organizational skills.
• Extensive knowledge of quality standards and regulatory requirements.
• Flexibility to adapt to changing assignments.
• Project management and communication skills.
• Ability to work independently or in a team.
• Strong interpersonal skills.

Benefits

• Comprehensive benefits package including paid time off.
• Medical, dental, and vision insurance.
• 401(k) eligibility.
• Participation in short-term and long-term incentive programs.