Receive regular GMP training, regulatory training, and company role training/assessments; attend data reliability training on schedule to strengthen awareness of data reliability
Job Summary
Receive regular GMP training, regulatory training, and company role training/assessments; attend data reliability training on schedule to strengthen awareness of data reliability.
Be responsible for physicochemical testing related to plasmids, lentiviral vectors, and CAR‑T; maintain and update relevant SOPs and records.
Comply with GMP (2010 Edition), “Drug Records and Data Management Requirements (Trial),” and company data integrity policies to ensure data integrity.
Matching Summary
Receive regular GMP training, regulatory training, and company role training/assessments; attend data reliability training on schedule to strengthen awareness of data reliability.
Skills & Requirements
Must-have
GMP compliant laboratory management
analytical methods SOP drafting
process water monitoring
material sampling and testing
quality event investigation
analytical method validation
Nice-to-have
embraces diversity and equality
inclusive and diverse team
strong communication skills
good English ability
Key Requirements
Associate degree or above
Three or more years of experience
Familiar with GMP regulations
Familiar with pharmaceutical physicochemical laboratory practices