The role requires leading daily manufacturing management including deviation investigations, CAPA, and change control while serving as the process owner during PPQ stages
Job Summary
The role requires leading daily manufacturing management including deviation investigations, CAPA, and change control while serving as the process owner during PPQ stages.
Candidates must support cross-border technology transfers to various CDMOs or production sites and ensure projects progress according to plan through close departmental collaboration.
The position involves conducting talent development and training work specifically focused on MSAT downstream processes within a GMP environment.
Matching Summary
The role requires leading daily manufacturing management including deviation investigations, CAPA, and change control while serving as the process owner during PPQ stages.
Skills & Requirements
Must-have
GMP production experience
Technical transfer expertise
Process performance qualification (PPQ)
Deviation investigation and CAPA
Change control management
Bilingual technical writing
Nice-to-have
Continuous process optimization
Cross-border collaboration skills
Talent development leadership
CDMO site coordination
Key Requirements
Bachelor's degree in Bioengineering or related field
MSAT/PD experience in biopharmaceuticals
Experience with tech transfer and process validation
Proficiency in reading/writing Chinese and English technical documents