AbbVie's Internal Audit & Inspection Management team needs support in assessing compliance and quality of R&D's pharmaceutical, device, and combination products GxP lifecycle standards to ensure continuous real-time inspection readiness.
Requirements
- Currently enrolled in university, pursuing a Bachelor’s degree in bioengineering, biomedical engineering, pharmacy, life sciences (e.g., biology or biochemistry), public health, nursing, health sciences, biomedical sciences, clinical research, business administration in a healthcare setting or auditing, regulatory affairs, or other related degree
- Medical device or project management experience
Responsibilities
- Support the Internal Audit & Inspection Management team in planning, organizing, and executing audits to independently assess compliance with AbbVie’s GxP lifecycle standards for pharmaceutical, device, and combination products.
- Assist with documentation review and data collation to verify adherence to regulatory and internal quality requirements during audits and inspections.
- Help identify and track trends in internal audit findings, contributing to ongoing knowledge management initiatives.
- Participate in the development and continuous improvement of processes to ensure real-time inspection readiness.
- Aid in the follow-up of CAPAs resulting from audit findings, supporting robust and proactive quality improvement.
- Contribute to the preparation of reports, presentations, and training materials summarizing audit outcomes and key learnings.
Other
- Currently enrolled in university, pursuing a Bachelor’s degree
- Must be enrolled in university for at least one semester following the internship
- Travel: Yes, 5% of the Time
- Expected graduation date between December 2026 – June 2027
