Participate in the daily inspection and management of the QC cell group, including work arrangements and tracking, and establishing a document system
Job Summary
Participate in the daily inspection and management of the QC cell group, including work arrangements and tracking, and establishing a document system.
Organize personnel to carry out release inspection and quality research inspection of materials, lentiviral vectors, and CAR-T samples according to the plan, ensuring the authenticity and reliability of inspection data.
The company embraces diversity and equality of opportunity, committed to building an inclusive and diverse team representing all backgrounds.
Matching Summary
Participate in the daily inspection and management of the QC cell group, including work arrangements and tracking, and establishing a document system.
Skills & Requirements
Must-have
QC cell daily inspection and management
Establish document system
Cell group laboratory normal daily management
CAR-T cell culture and efficacy testing
Flow cytometry basic operations
Analytical method validation experience
Nice-to-have
Adapt to fast-paced industry
Low error tolerance required
Strong stress resistance
Willingness to adapt to shifts
Key Requirements
Bachelor's degree or above
3+ years of QC experience in biopharmaceutical industry
2+ years of GMP environment experience
CET-6 or above English proficiency
Cell therapy related experience preferred
T cell and HeLa cell line culture experience preferred
BD Canto or Lyric flow cytometer experience preferred
CAR-T cell culture, efficacy, and flow related testing experience preferred
Experience in handling OOS and deviation quality events preferred