Elisabeth Lidholm

• I am analytical chemist and pharmacist (MSc Pharm), • Have long experience of pharmaceutical projects, both from early and late phases. • Broad experience from oral and inhalation projects. • Has worked as Substance Coordinator. As a Substance Coordinator I was responsible for drug substance characterisation, which means to ensure that all needed information about the drug substance was collected. The coordinator role included laboratory work, documentation work and collaboration with colleagues from different parts of the organisation (e.g. Specialists, process R&D, project leaders). • Very experienced in analytical techniques as UHPLC, HPLC, TGA, DSC and automated inhalation techniques. Experience from techniques as GC, KF, XRPD and TLC. Speciality: UHPLC/HPLC • Very experienced in method development/validation, stability studies, performing and documenting laboratory work according to GMP/GLP, authoring the CMC part of clinical trial applications/registration files, specifications. • Worked with Lean Sigma projects. Key qualities: Team player, thorough, flexible, have a curiosity in learning new things.