At Merck AG Switzerland, I lead chromatography laboratories for HPLC, GC, and TLC in GMP, ISO 13485, and ISO 9000 environments. I coordinate analytical testing orders, review chromatography data and reports, and manage reference standards for APIs and excipients.
I develop and implement HPLC and GC methods, introduce pharmacopeial methods according to Ph. Eur. and USP, and plan instrument qualifications. My work also includes deviation root cause analysis, change control, complaint handling, and re-test planning.
Previously at Weidmann Medical Technology, I qualified production and measuring equipment, validated manufacturing and measurement processes, and supported medical products from project phase through series production. I also qualified ISO Class 8 and 9 cleanrooms and performed FMEA-based risk analyses.
I'm a chemistry graduate from ZHAW with hands-on lab informatics experience across Chromeleon CDS, LIMS/ELN/LES, GMP, CSV, SQL, PowerShell, Bash, Python, R, and MATLAB.
