Reviewer Durban - eThekwini
Scribante Labour Consultants
To ensure optimal batch document and related documents review in accordance with cGMP and execute all relevant administrative tasks Audit BMRs, BPRs, Protocols and other process related documents for completeness and compliance to GMP and regulatory. Ensure all points on the ‘production batch completion checklist' is verified. Identify document audit queries and resolve by engaging with relevant operators, pharmacists, supervisors and other staff, members related to the completion of such processing documents. Tracking and monitoring of frequent/ common document audit findings and reporting it to the supervisors, pharmacists as well as responsible staff member for the audit finding. Auditing of BMRs/ BPRs must done accordingly to the sequence in which the jobs are complete, or prioritized as per the planned release and dispatch schedule. BMRs, BPRs and other processing documents must be logged in at QA offices Receipting of complete jobs onto Syspro, reporting and investigating variances on jobs and the closure of jobs on the system. Ensuring all bulk product samples are forwarded to the Quality Control laboratory, and all relevant records and documentation is complete. Communication to all relevant departments on jobs complete on a daily basis. Ensure all work in progress BMRs/ BPRs are correctly stored in the office The drawing up and typing of all relevant documents as requested by the production supervisors, pharmacist or manufacturing manager. Capturing of daily production activities, to facilitate monthly production stats reports To assist other administrators with job specific task as and when required. Carrying out general errands and general instructions delegated by supervisors/ pharmacist and department manager. Matric and related tertiary qualification Computer Literacy Minimum 3 years experience in a pharmaceutical manufacturing environment Pharmacist Assistant Basic will be advantageous
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