Production Administrator

Guided by its purpose to provide products for patients to alleviate pain and suffering and improve their quality of life, NBI’s vision is to be the leading African manufacturer and supplier of quality therapeutic proteins and diagnostic products.

• Verification of MCD’s and collection from QA.
• Ensure correct filing of MCDs as per status of the batch in a timeous manner
• Compilation and review of MCDs to ensure completion
• Confirmation and Goods Receipt of product yields on SAP for Pharmacist verification
• Pre-audit of MCD as per checklist prior to pharmacist audit.
• Check that all calculations and formulations in the document are correct before pharmacist audit
• Submission of MCDs to ORP following pharmacist audit. Compilation of the final batch document to include all the reports and results of QC testing.
• Recording status of MCDs in log books when submitted to ORP. Ensure MCDs are received and acknowledgement of receipt completed on log book. Management of the Document Tracing Register for accuracy to ensure traceability
• Recording/tracking of MCD status until submission to ORP
• In-process monitoring of the batch documentation to ensure that all mandatory information is completed and verified.
• Follow up on MCD status for any queries where necessary
• Action all document queries to the relevant pharmacists, section heads and technicians
• Attend to MCD queries where possible.
• Maintain document release target of two weeks from production to ORP.
• Compilation of in-process data controls for product investigations

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