Stockholm, Stockholm County, Sweden
Analytical Chemist with strong experience in pharmaceutical R&D, quality control, and method development in GMP/GLP environments. I have hands-on expertise in LC-MS/MS, HPLC/UPLC, and GC-MS, with a focus on method development, validation (ICH guidelines), impurity profiling, and stability studies. My work includes both small molecules and biomolecular systems, including peptide-related analyses. I have worked in both academic and industrial environments, contributing to analytical workflow development, formulation support, and data-driven characterization of complex systems. Key expertise: • LC-MS/MS, HPLC/UPLC, GC-MS • Method development & validation (ICH Q2) • QC / GMP / GLP environments • Stability testing & impurity profiling • Biomolecular & pharmaceutical analysis • DoE and data-driven optimization I am currently based in Sweden and open to opportunities in Analytical R&D, Pharmaceutical Development, and Quality Control.
• Designed and executed experiments for analytical and formulation development. • Performed protein and small molecule characterization using HPLC, GC, DSC, and spectroscopy. • Developed robust analytical methods in GMP environment. • Authored SOPs, reports, and regulatory documentation. • Collaborated across R&D and QC teams for process development and validation.
Modeled and analyzed pollutant data using R to support environmental research projects. Conducted chemical and physical analyses using spectroscopy, GC, HPLC, LC-MS, UV/Vis, and ELISA. Developed and validated analytical methods, ensuring compliance with regulatory standards (GMP/GLP). Managed deviations, CAPAs, and documentation in alignment with quality requirements. Collaborated with cross-functional teams to optimize processes and support research outcomes.
• Developed analytical methods (HPLC, LC-MS/MS) for biomolecule characterization. • Designed experiments for protein and polymer-based systems. • Performed sample preparation and optimization of chromatographic workflows. • Maintained GLP/GMP-compliant documentation and reporting.
• Conducted quantitative analysis and developed innovative material strategies for environmentally friendly analytical methods. • Utilized advanced techniques such as HPLC, GC, UV/Vis, and XRD to improve process efficiency and accuracy. • Managed regulatory documentation and ensured GMP compliance while collaborating with external stakeholders.