GP

George van Parys

Global Quality Investigator, Lead Validation Engineer at Xellia

George Van Parys has over 15 years of experience in various roles in the pharmaceutical and engineering industry. George has worked as a Global Quality Investigator and Lead Validation Engineer at Xellia Pharmaceuticals since 2016. Prior to that, they were a Senior Consultant at ProPharma Group, where they handled specifications for new equipment and packaging materials. George also served as a Senior Packaging Engineering Consultant at KaVo Kerr Group, Gilead Sciences, and Teva Pharmaceuticals, where they worked on packaging design, validation, and qualification activities. In addition, George has experience as a Project Manager at Ben Venue Laboratories, where they led commissioning and qualification projects. George has also worked on automation and robotics systems design at Vestas and served as an Operations Manager at DMS Engineering, where they focused on packaging line redesigns and FDA compliance. George's expertise includes equipment modification, fabrication, augmentation, and project management.

George Van Parys attended LaSalle College, Temple University, Spring Garden College, and Thomas Edison College from 1977 to 1983. George obtained multiple degrees during this period, including a BSEE, BSIEE, BSIE, BSTGE, BSCS, and BSELE. The specific field of study for these degrees is not mentioned. Additionally, they also pursued degrees in Automation, Robotics, and Pharmaceutical, earning a BSEE, BSCS, BSELT, BSIE, and BSIEE.

Links

Previous companies

Gilead Sciences logo
Teva Pharmaceutical Industries logo
Integra LifeSciences logo
ProPharma Group logo
Vestas logo

Timeline

  • Global Quality Investigator, Lead Validation Engineer

    March, 2016 - present