Responsible for the inspection and related work of QC laboratory original and auxiliary materials and packaging materials, including establishing and maintaining quality standards, inspection procedures, and detection methods.
Requirements
- At least 5 years of experience in detecting original and auxiliary packaging, with priority given to those with relevant experience in the biopharmaceutical industry
- Ability to master various material detection methods, such as chemical identification, content, and impurities
- Familiarity with the Chinese Pharmacopoeia, GMP guidelines, and ICH guidelines for original and auxiliary material management, as well as foreign pharmacopoeia such as EP and USP
- Fluent English language skills in reading, speaking, and writing
- Good professional ethics and teamwork skills
- Familiarity with using Microsoft Office software (MS-Word, MS-Excel, MS-Outlook, etc.)