ISO 14644 Cleanrooms and associated controlled environments
USP 61 and USP 1111 Microbial Purity/bioburden
GMP
Pharmaceutical Industry
FDA
ISO 17025 Quality System Labor
AAMI 72/USP 85 Bacterial Endotoxin
ISO 17664 and ISO 11134, Instruments Reprocessing
Product Launch
Biotechnology
Cross-functional Team Leadership
Iso 11737 Sterilization
Instruments Reprocessing
Usp 61 and Usp 1111
Iso 11137 Radiation
Fda Glp
Iso 11737 Sterilization of Medical Devices Microbiological Methods
Validation
Medical Devices
Usp 62 Microbial
Iso 17664 and Iso 11134
Iso 11135 Eto
V&V
Iso 10993 Biological
Cross Functional Team Leadership
Iso 17025 Quality
Aami 72/Usp 85
Product Development
21 Cfr Part 58
Iso 17664 and Iso
R&d
Iso 14644 Cleanrooms
Ciming Li Summary
Ciming Li, based in Ennetbaden, AG, CH, is currently a Head of Process Validation Microbiology at SKAN. Ciming Li brings experience from previous roles at DSM, QS Zürich AG Zertifizierungen, CE, Medical Device and BIOTRONIK. Ciming Li holds a 2006 - 2006 Postdoctoral Scientist in Space Biology @ ETH Zürich. With a robust skill set that includes ISO 13485, CAPA, Quality System, ISO 11737 Sterilization of medical devices -- Microbiological methods, Quality Control and more. Ciming Li has 3 emails on RocketReach.
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