Sandrine Benguira holds a Master of Science in Biology with a specialization in Endocrine Toxicology and a Bachelor of Science in Biology with concentrations in Toxicology and Physiology from Université du Québec à Montréal. She is a senior quality and compliance consultant with 27+ years of experience in the pharmaceutical, biotechnology, medical device, natural health product, and clinical research industries. 

Sandrine supports life-sciences organizations in building, strengthening, and sustaining effective Quality Management Systems and achieving robust GMP and regulatory compliance. Her consulting work spans GMP compliance, QMS development and remediation, quality-system optimization, inspection readiness, and regulatory oversight.

A defining strength of Sandrine’s approach is her ability to bridge quality, operations, regulatory expectations, and organizational leadership. She views GMP compliance as an operational discipline, not a documentation exercise, and brings extensive hands-on experience in investigations, risk-based problem solving, continuous improvement, supplier oversight, quality-system governance, inspection preparation, and cross-functional leadership.

Her technical expertise covers GMP, GCP, ISO 13485, ISO 14971, quality-system management, CAPA, root-cause analysis, change control, deviations, vendor management, audits, inspections, product release, clinical research compliance, and quality documentation. 

Today, Sandrine provides senior-level guidance to organizations seeking to build a compliant QMS structures, remediate quality-system gaps, prepare for regulatory inspections, strengthen GMP operations, resolve complex quality issues, enhance supplier oversight, and implement sustainable quality processes.