Lotte is a CQV Lead with 6 years of experience within production, compliance, and document control, bringing a strong GMP mindset from roles in both pharma and biotech. She has managed CQV activities, operation readiness, and quality documentation for complex projects, including rebuilds of facilities, utilities, and production equipment.
With a Project Management certification and a proven track record in deviation handling, process optimization, and stakeholder coordination, Lotte thrives in dynamic environments where structure and problem-solving are key. She combines technical insight with a positive, can-do attitude, ensuring smooth execution and regulatory compliance.
