2026 Quality Assurance & Compliance Intern (Graduate)

Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Job Description

As a QA & Compliance Intern at AbbVie, you will spend your summer engaged with energetic colleagues and inspirational leaders, gaining world-class experience within one of the most dynamic organizations in the pharmaceutical and medical device industry. 

You will support the R&D Quality Assurance & Compliance team, which develops, implements, and continually improves the AbbVie Quality System in R&D. The team ensures that clinical research and operations consistently meet regulatory requirements, internal standards, and ethical guidelines, thereby protecting patient safety, upholding data integrity, and supporting the reliable development and approval of products. 

Key Responsibilities:

• Independently review complex clinical trial and regulatory documents for compliance with regulatory standards and internal quality requirements. 

• Contribute to the design, optimization, and continuous improvement of quality processes and systems within R&D. 

• Analyze quality metrics, interpret data trends, and prepare informative summaries or reports for the team and drive analytics and AI programs 

• Take an active role in drafting, updating, and reviewing standard operating procedures (SOPs) with attention to regulatory context and process effectiveness. 

• Participate directly in audit preparation, execution, and post-audit follow-up, including drafting sections of audit reports as appropriate. 

• Lead or co-lead assigned projects or process improvement initiatives under supervision. 

• Collaborate cross-functionally with clinical, regulatory, and oper