Beschreibung

You will strengthen global health by harmonizing regulatory systems and building regional manufacturing capacity. Your work ensures safe access to medicines through expert QA advice and strategic partnerships.

Anforderungen

• •Advanced degree in health science or equivalent
• •Certification in regulatory affairs
• •QA management experience in public/private sector
• •Experience with QA regulatory policies and frameworks
• •Experience with external partner engagement
• •Knowledge in developing QA policies and tools
• •Experience in matrix organizations and cross-functional teams
• •Minimum 6 years experience in QA/regulatory affairs
• •Work experience in Global Fund supported countries
• •Excellent English and good French knowledge
• •Ability to lead and collaborate in teams

Aufgaben

• •Support regulatory systems and quality assurance implementation
• •Manage registration, storage, and distribution requirements
• •Oversee market surveillance and quality control testing
• •Select service providers for regulatory and QA matters
• •Build regional manufacturing capacity and regulatory strengthening
• •Develop the Global Fund Regulatory Systems blueprint
• •Review funding requests to enhance country QA capacities
• •Coordinate supply operations for aligned regulatory approaches
• •Partner with authorities on regional harmonization and reliance
• •Integrate QA management systems with enterprise resource tools
• •Enhance QA policies, guidelines, and governance models
• •Advise stakeholders on country QA maturity assessments
• •Identify system weaknesses and capacity gaps
• •Create technical briefs for funding request applicants