· Participate in initial and quarterly GMP audits for pharmaceutical
manufacturers.
· Compile all technical reports and follow up closely with manufacturers
to ensure timely implementation of CAPAs.
· Support the Technical Advisor, CMC, to close gaps identified during audits.
· Lead technical assistance to compile/finalize CTD product dossiers for
submission to Ghana FDA and/or WHO.
· Lead all routine or ad-hoc technical day-to-day check-in meetings with
manufacturers based in Ghana.
· Lead advocacy meetings with industry stakeholders within Ghana’s
pharmaceutical sector.
· Co-facilitate a national-level workshop to
introduce and promote use of the industry ‘playbook’ among manufacturers,
regulators, and other stakeholders.
· Design and deliver GMP and Quality Management
System (QMS) trainings for regulatory professionals and industry staff across
the region.
The U.S. Pharmacopeial Convention (USP)
is an independent scientific organization that collaborates with the world's
top experts in health and science to develop quality resources and standards
for medicines, dietary supplements, and food ingredients. Through our
resources, standards, advocacy and education, USP helps increase the
availability of quality medicines, supplements and foods for billions of people
worldwide. Our programs have reached more than 90 countries across Africa,
Asia, and South America to strengthen global supply chains and pharmaceutical
ecosystems that enable a resilient supply of quality medical products.
