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Jesper Brandt Rasmussen

Senior Consultant

Design Control
Test & Verification
Data Visualization
Project Management
Medical Device Development
SAS JMP
Stakeholder management
GMP
Risk management
IVDR/MDR
Quality review and documentation
Validation testing
21 CFR Part 11
ISO 10993-1 & ISO 13485
Equipment validation

Jesper Brandt Rasmussen holds as M.Sc. in Chemical Engineering from the Technical University of Denmark.

Jesper has more than 10 years of experience from the Life Science industry as both a consultant and an employee. He has built up solid competencies within the development of medical devices, as well as the preparation of quality documentation within the pharmaceutical and MedTech industry. This applies in particular to Design Control deliveries, testing and verification activities, requirement specifications and validation documentation.

As a consultant, Jesper makes a virtue of doing his job systematic, conscientiously and with high integrity. Both when it comes to communication, collaborative relationships and task execution.

I bring things into order and discover the errors and shortcomings that occur based on concrete facts. I use it on a daily basis when I have to advise and execute on projects, in order to add as much value as possible to the deliveries. I like to spice it up with humor, add a sprinkle of technical ingenuity and bake it with appropriate pragmatism.”