Kirsten Graa Thomsen

Senior Consultant

Relevant job experience

 

Before joining Qmed consulting Kirsten has 12 years experience with quality assurance and regulatory affairs as QA Coordinator and QA Manager covering pharmaceuticals and medical devices. Building up and maintaining quality systems based on GMP, ISO 13485 and ISO 9001. She has worked in companies of different sizes covering all aspects of quality assurance. In the small companies she has worked with both Quality and Regulatory issues during development and production. Kirsten has also functioned as Qualified Person for some of the companies and has documented qualification as Internal Auditor.

 

Furthermore Kirsten has more than 20years experience in evaluation of occupational health with main focus on toxicology and work related allergy and hypersensitivity prior to joining Qmed Consulting. She has worked for 10 years at the national institute of Occupational Health dealing with allergy and other chemically induced health problems.

 

 

During all years she has been working with adult education and training in many aspects concerning quality assurance and work environment. In addition she has performed compendia, booklets, articles and teaching materials about the issues.

 

Education

M Sc in biology from the University of Copenhagen with speciality in immunology.

 

This has been supplemented with several courses in toxicology and quality assurance.