QMS Administrator
Core
Administer and optimize enterprise Quality Management Systems (QMS) to ensure compliant, efficient document and quality processes for manufacturing medicines.
Role type
QMS Administrator (Site-based)
Builds
Enterprise QMS workflows, document lifecycle processes, and audit-ready systems
Domain
Life Sciences / Pharmaceutical Manufacturing / Quality Assurance
Deliverable
production ML models | product features | dashboards & analysis | infrastructure
Required skills
System configuration, workflow design, data migration, regulatory compliance interpretation, user access management, SOP development
Preferred skills
Experience with Documentum, TrackWise, SharePoint, LIMS, Empower
Technologies
Documentum, TrackWise, SharePoint, LIMS, Empower
Responsibilities
Configure and maintain QMS workflows for document lifecycle and approvals; Lead data migration activities including mapping and validation; Manage system users, roles, and permissions; Collaborate with Quality, IT, and Manufacturing teams; Support system testing, audits, and inspections; Develop SOPs and quality metrics
Seniority
Mid-Senior, hands-on IC
