SOQ Senior Associate
Core
Ensure compliance with Pfizer and Regulatory Authority expectations by supporting, maintaining, and implementing the Quality Management System (QMS) at Country Offices, managing product disposition, and overseeing supplier quality.
Role type
Senior IC Quality Assurance Associate (Pharmaceuticals)
Builds
Quality Management Systems (QMS), compliant product supply operations, and regulatory inspection readiness
Domain
Pharmaceuticals / Life Sciences / Quality Assurance
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
GxP regulations knowledge, deviation investigation, CAPA management, change control, supplier qualification, audit coordination, root cause analysis, KPI monitoring, product release/disposition
Preferred skills
Project management, root cause analysis methodology, regulatory affairs background, higher degree in Life Sciences
Technologies
Microsoft Excel, Microsoft Word
Responsibilities
Lead deviation investigations and implement CAPAs; Manage product release, repackaging, and relabeling; Execute supplier quality management tasks; Coordinate internal audits and Health Authority inspections; Monitor QMS KPIs and trends; Facilitate project initiatives and quality culture development
Seniority
Senior, hands-on IC