Malmo, Skåne County, Sweden
Experienced chemist with an analytical approach to any issue and a demonstrated history of working in the pharmaceuticals industry. Positive, and always striving for improvement. A reliable, responsible and ambitious team-player.
• LabWare LIMS 8 system administrator • Responsible for the implementation of the continuous monitoring system, Vaisala viewLinc • Method validation and stability testing according to ICH guidelines • Analyses of raw materials and semi-solid/liquid products • Experience with LIMS and Chromeleon
• Verification of pharmacopoeial methods • Analyses of raw materials for solid/polymer products • Experience with silicone measurements
• Product- and project responsibility • Method establishment and stability testing according to ICH guidelines • Pharmacopoeia-, reference standard- and instrument responsibility • Administrator of instrument software • Write SOP, methods, stability protocols, reports and cleaning validation • Analyses of packaging materials, raw materials, APIs and aseptic/non-sterile products • Everything within the framework of GMP and the analyses are performed according to pharmacopoeial methods (Ph Eur, USP, JP, BP) and internal methods • Experience with Empower, HPLC, GC, FTIR, UV-Vis, wet chemistry, etc