We’d like to welcome QA Consulting’s new Senior Quality and Microbiology Consultant, Adrienne Schroll!
We’re thrilled to introduce Adrienne Schroll, a proven Quality and Regulatory Affairs leader with 17+ years of experience across the medical device, pharmaceutical, and combination product industries.
Adrienne has driven quality strategy, regulatory compliance, and QMS implementation across Class I–III devices—including active implantable and sterile single-use products—ensuring alignment with ISO 13485, FDA 21 CFR 820, EU MDR/MDD, MDSAP, and the evolving QMSR. Currently serving as Director of Quality and Regulatory at Interrad Medical and Principal Consultant at Schroll Quality Consulting, she specializes in CAPA, design control, risk management, supplier quality, and regulatory submissions. With deep technical expertise in microbiology, sterilization validation (ISO 11135/11137), and contamination control, Adrienne has successfully led teams through global audits and inspections while building high-performing teams and future-ready quality systems. Holding a Master’s in Regulatory Affairs and Quality Assurance from Temple University, she combines strategic vision with hands-on execution to drive compliance, innovation, and market success.
Welcome to QA Consulting, Adrienne! We’re excited to have you join our team!
Lean into our quality and microbiology expertise by scheduling a discovery call today!
