Start of professional career as the head of QC department of a HK based pharmaceutical company. Since 2001, working in deep consideration of GMP relevant processes and products on the development and analysis of chemical pathways and procedures mainly with the focus on the production of life science products.

Joono has 10 plus years of experience in GMP and GMP related processes. She actively worked on numerous Chinese GMP projects doing trainings and consultancy on topics like risk assessment, SOP preparation and handling, qualification and validation, and many more. She guided a lot of western auditors doing GMP compliance audits and executes 3rd party audits by herself. She is expert in Chinese and western (EU/ US) GMP guidelines respectively and also is involved in CEP/ ASMF/ DMF preparation and filing. She gave several trainings and lectures directly for pharmaceutical companies as well as during public seminars.