QC Supervisor
Core
Coordinate daily laboratory activities, lead a team of QC analysts, and ensure compliance with GMP and regulatory requirements to support product release.
Role type
Senior IC Quality Control Supervisor
Builds
Influenza vaccines and other pharmaceutical products
Domain
Pharmaceutical / Biotech / Regulated Industry
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
cGMP compliance, laboratory supervision, root cause analysis, SOP development and review, data review and approval, equipment validation, change control management, KPI monitoring, team training and development
Preferred skills
Continuous improvement techniques, advanced root cause analysis, FDA and EMA regulatory knowledge, creative problem solving within cGMP constraints
Technologies
Chemical testing instruments, validated test processes, laboratory information systems
Responsibilities
Supervise daily laboratory activities and ensure compliance with quality standards; Schedule team activities and manage holidays, sickness, and training; Review and approve test data, protocols, and reports for adherence to cGMPs; Investigate aberrant results and determine root causes; Coordinate SOP development, review, and approval; Ensure maintenance and qualification of laboratory equipment; Lead troubleshooting of testing problems and participate in improvement projects; Monitor team performance and mandatory training compliance
Seniority
Senior, hands-on IC
