Rob Van Blijswijk

Rob Van Blijswijk

Sr. Quality Engineer Ii Quality And Automation @ Kite Pharma

About Rob Van Blijswijk

Rob Van Blijswijk is a Sr. Quality Engineer II specializing in Quality and Automation at Kite Pharma in Hoofddorp, Netherlands, with extensive experience in laboratory IT and quality oversight across various pharmaceutical and research organizations.

Work at Kite Pharma

Rob Van Blijswijk currently serves as a Senior Quality Engineer II in Quality and Automation at Kite Pharma, a position he has held since 2022. His role involves providing quality oversight for various systems, including Manufacturing Execution Systems (MES) and Laboratory Information Management Systems (LIMS). Prior to this position, he worked at Kite Pharma as a Senior Quality Engineer focusing on LIMS, MES, IT, and Computer System Validation (CSV) from 2021 to 2022. His tenure at Kite Pharma has been characterized by a commitment to ensuring compliance and operational efficiency within the organization.

Previous Experience in Quality Engineering

Before joining Kite Pharma, Rob Van Blijswijk accumulated extensive experience in quality engineering and IT consultancy roles. He worked at Rescop as a Senior Laboratory IT Consultant, specializing in LIMS and CSV for six months in 2019. Additionally, he served as a Quality Systems Manager at MSD Netherlands for eight months, where he focused on aligning quality systems with business processes. His background includes roles at various organizations, including Crucell and Teva Pharmachemie, where he contributed to quality assurance and IT system management.

Education and Expertise

Rob Van Blijswijk holds a Bachelor's Degree in Business ICT & Management from Haagse Hogeschool Den Haag, which he completed from 2011 to 2014. He also studied Microbiology at Reijnevelt College in Delft, achieving an MBO+ qualification from 1987 to 1992. His educational background supports his expertise in aligning business processes with IT systems and ensuring compliance with Good Manufacturing Practice (GMP) regulations. He possesses a comprehensive understanding of data integrity and compliance with 21 CFR Part 11 regulations.

Background in Laboratory IT and Automation

Rob Van Blijswijk has a robust background in laboratory IT and automation spanning several years. He worked as a Laboratory Automation Specialist at DSM Research for 11 years and as an Application Support Specialist at Labtronics for three years. His experience includes providing quality oversight for systems such as LIMS, EMS, and QC instruments. He has also held positions that required him to ensure compliance with GxP and ISO standards, demonstrating his capability in regulated environments.

Career Progression and Roles

Rob Van Blijswijk's career reflects a steady progression through various roles in quality engineering and IT consultancy. He has worked in multiple organizations, including Intertek, GD (Gezondheidsdienst voor Dieren), and AQUON, where he contributed to the implementation and management of laboratory information systems. His diverse experience across different sectors has equipped him with the skills necessary to enhance operational efficiency and maintain compliance in pharmaceutical and laboratory settings.

People similar to Rob Van Blijswijk