Stability Supervisor 2
Core
Overseeing quality records, managing corrective and preventive actions, and leading investigations to ensure compliance and continuous improvement in a pharmaceutical manufacturing stability environment.
Role type
Senior IC stability supervisor (quality)
Builds
Product integrity and optimized shelf-life predictions throughout the product lifecycle
Domain
Pharmaceutical manufacturing / Quality Assurance
Deliverable
production ML models | dashboards & analysis | client delivery
Required skills
stability protocols, CAPA processes, regulatory compliance, data analysis, team leadership, change control, OOS/OOT investigation, statistical software, Microsoft Office (Excel, PowerPoint)
Preferred skills
AI and machine learning integration, ICH guidelines, GMP standards, syndicated data analysis, project management
Technologies
predictive analytics models, data visualization tools, statistical software, Microsoft Office
Responsibilities
Lead and innovate stability protocols; supervise and mentor quality specialists; collaborate cross-functionally with R&D and Manufacturing; drive compliance with global regulatory standards; analyze stability data to identify trends; champion sustainability initiatives; utilize data visualization tools for stakeholder reporting; oversee maintenance of quality records; review and approve laboratory data; perform investigations on OOS/OOT results; provide technical direction and training to scientists.
Seniority
Senior, hands-on IC with team leadership
