Clerk-Data Entry CRC

The Clerk - Data Entry provides administrative and technical support to the ACTC team and particularly takes responsibility for Good Manufacturing Practice (GMP) Laboratory Data Entry related of therapeutic product preparation. The Clerk tracks non-conformities for ISO 9001;2015 Quality Management System. S/he is primarily responsible for data collection and entry, monitoring the data and reporting them to the ACTC team; preparing and processing necessary documents for licensing applications; monitoring and updating the log report for the inventory and products; performing general office support; preparing MoM. The incumbent prepares purchase requisitions and documents and channels them for approvals. KEY ROLE ACCOUNTABILITIES Clinical related activities support • Data collection, archiving, monitoring of the GMP laboratory, related to: • bone marrow harvest support and harvest processing for hematopoietic transplant therapy. • Cord blood and peripheral harvest cell processing for hematopoietic transplant therapy. • Peripheral blood and other tissues processing for regenerative medicine products. • Tissue and cell processing for cell and gene therapy. • Takes care of the GMP storage room for reagents and consumables, in terms of stock control and activation purchase request for replenishment. Tracks the placed orders, stock arrival and ensures stock count is continuously updated. • Participates and follows Certification and Accreditation requirements related to: JCI international accreditation standards, ISO quality and technical standards, JACIE-FACT accreditation standards, GMP guidelines, etc. Supports certification achievement during all the certification or accreditation cycles. Actively participates in Quality Improvement Programs