With more than 30 years of experience from various roles within product development of pharmaceuticals, Lena is a proficient and trustworthy colleague with experiences from working both as SME, Process Engineer and QA Engineer. Starting with a Master of Science in Biochemestry, Lena throughout the years by working with formulation of products used for phase I, II and III clinical trials, as well as commercial production, has gained great experience and formulating knowledge in over-encapsulation, nano-, micro- suspensions, transdermal formulations as well as tablets and capsule formulations. Lena also has good knowledge of microbiological aspects and risk assessment for formulations during the development process. Additionally, Lena well knows how to monitor products and processes to meet regulations from authorities and has great experience in writing documentation and instructions for clinical trials, as well as commercial products. With a vast experience from GMP facilities and equipment related projects, Lena has carried out tasks such as purchasing, URS, and writing IQ/OQ/PQ/PV protocols and reports. She also has experience as SME for GMP production and validation. Lena has good knowledge in GDP, (good documentation practice). As a person and colleague Lena has a positive and can do-mindset with great focus on creating the most sustainable, and at the same time profitable, solution for any given situation, product, or process.