삼성바이오로직스 · yesterday
QA Specialist (GMP 품질보증)
Why it fits
- Reviewed 400+ mAb drug-substance batch records a year at Celltrion — the core of this role
- Hosted 6 FDA/EMA/MFDS inspections, matching the audit-response requirement
Watch-outs
- No PMDA (Japan) inspection on your resume — bridge from your other inspections in the interview