[QA] System 경력사원 채용
Core
Operate Quality Deviation and Change Control systems, manage document control regulations, and ensure data integrity in a laboratory setting.
Role type
Senior Quality Assurance System Specialist (GMP)
Builds
Quality management systems and compliant laboratory operations
Domain
Pharmaceutical/Manufacturing Quality Assurance
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
GMP project management, data integrity assurance, raw material management, supplier qualification, audit response, change control management, deviation management
Preferred skills
QC system experience, chemical/microbial lab experience, US FDA PLI inspection experience, EU inspection experience, fluent English communication
Technologies
GMP systems, Change Control systems, Deviation management tools
Responsibilities
Manage Quality Deviation and Change Control systems, upgrade document control regulations, optimize Contamination Control Strategy (CCS), conduct supplier qualification audits, lead GMP upgrade projects, respond to government and customer audits
Seniority
Senior, hands-on IC
