Supervisor, Quality Systems
Core
Supervise daily execution of Quality Systems processes and activities to ensure GMP compliance and inspection readiness for pharmaceutical manufacturing operations.
Role type
Senior IC Quality Systems Supervisor
Builds
Quality Management System (QMS) processes, records, and compliance frameworks
Domain
Biopharma / Pharmaceutical Manufacturing / Quality Assurance
Required skills
GMP regulations knowledge, deviation/investigation/CAPA management, document control, audit/inspection support, team supervision, KPI reporting, cross-functional collaboration
Preferred skills
Bachelor's in Life Sciences, experience in sterile/biologic manufacturing, proficiency in electronic QMS tools, prior supervisor/lead experience
Technologies
Electronic Quality Management Systems (eQMS), Quality-data reporting tools
Responsibilities
Supervise daily execution of assigned Quality Systems processes and activities; Ensure quality records are complete, accurate, timely, and maintained in an inspection-ready state; Coordinate the review, approval, tracking, and closure of QMS records; Assign work, establish priorities, monitor progress, and escalate risks; Provide coaching, technical guidance, and performance feedback to team members; Support implementation and continuous improvement of site QMS procedures; Partner with Manufacturing, QC, Validation, and Engineering to resolve quality-system issues; Support Quality KPI data collection, verification, reporting, and trend analysis; Support client requests, audits, regulatory inspections, and inspection-readiness activities.
Seniority
Senior, hands-on IC with team leadership
