Experience Built Across Science, Manufacturing & Projects

Klentz Consulting was founded to provide practical, specialist support to pharmaceutical and biopharmaceutical organisations, combining scientific understanding with hands-on manufacturing and project experience.

With experience spanning biopharmaceutical manufacturing, GMP operations, large-scale pharmaceutical projects and manufacturing planning, Klentz Consulting brings a broad perspective to complex challenges — from the technical details of an operation to the coordination required to deliver a project successfully.

Scientific & Technical Foundation

I hold an MSc in Human Biology from the University of Copenhagen, with a focus on areas including microbiology, molecular biology and immunology. My academic and research experience has provided a strong scientific foundation that I bring into practical manufacturing and operational challenges.

Biopharmaceutical Manufacturing

At AGC Biologics, I worked within upstream biopharmaceutical manufacturing, supporting mammalian cell culture and perfusion processes in a GMP environment. The role involved manufacturing operations, process support, documentation and cross-functional collaboration, providing hands-on experience from the production floor.

Pharmaceutical Manufacturing & Project Management

At Novo Nordisk, I worked as a Project Manager within large-scale pharmaceutical manufacturing, supporting projects related to manufacturing capacity, technical infrastructure and production requirements. The work involved coordinating cross-functional teams, managing complex project activities and working within a highly regulated GMP environment.

The experience provided a strong understanding of how large pharmaceutical manufacturing projects are planned and executed — from defining requirements and coordinating stakeholders to implementation, capacity expansion and operational readiness.

Manufacturing Planning & Resource Management

I currently provide consulting support within pharmaceutical manufacturing, focusing on manufacturing scheduling, resource planning and operational coordination in a GMP-regulated environment. The work involves translating manufacturing requirements into practical plans, coordinating resources and supporting day-to-day operational decision-making.

This experience provides a direct connection between hands-on manufacturing knowledge, project management and the practical planning required to keep complex manufacturing operations running effectively.