Case Study
Tuesday, September 23
05:45 PM - 06:10 PM
Live in Berlin
Less Details
This session will provide a deep dive into Lonza’s approach to establishing and sustaining a global MES support organization. The discussion will highlight how the company has approached structuring teams, harmonizing processes, and embracing a culture of continuous improvement to enhance operational efficiency and system reliability across multiple sites and time zones. In this session, you will learn how to:
Supporting (BIO) Pharmaceutical and Medical Device Companies
Providing operational support for MES software in a GMP (Good Manufacturing Practices) regulated environment, including:
Software deployment
Incident management
Problem management
Lifecycle management
System maintenance
Training
Validation (GAMP5, Computerized Systems Validation)
Responsibilities also include managing application upgrades, projects, enhancements, and security patches.
I bring comprehensive IT and automation integration expertise, combined with strong communication skills in Dutch and fluent English (both verbal and written). This enables me to effectively liaise with customers, vendors, and IT and engineering experts (e.g., application, network, database specialists) locally and across multiple sites. I excel at translating technical concepts into user-friendly language, bridging the gap between business and IT.
I am accustomed to adhering to GMP/GCP procedures and ensuring that new systems are implemented in compliance with FDA/EMA and other regulatory requirements. My experience includes working in global, cross-functional, and virtual teams across different time zones.
Proficient in developing and executing SOPs, as well as Installation and Operational Qualification (IQ/OQ) protocols, I have a solid understanding of FDA GxP and 21 CFR regulations. I am also well-versed in software system validation and working with solution lifecycle methodologies, such as Agile.