1. I maintain the quality management system and ensure that all the system documentation, procedures, SOPs batch product records are timely updated distributed and filled.
2. I report the status of quality compliance of staff, systems products and participate in internal audits corrective actions and carrying out investigations /report when necessary.
3. I participate in the evaluation of quality event, incidents, products complains, and follow up of activities in quality assurance department/ cGMP training.
4. I keep up to date with CGMP/compliance issues and retention of all products samples.
5. I develop packaging materials test for approval participate in suppliers/LASEPA visits. NAFDAC approvals and I represent Emzor Pharm. Industries in (M.A.N) Manufacturing association of Nigeria Isolo branch.
6. I monitor production processes, supervise In-process unit and Hygiene units respectively to ensure efficiency (25 staff).
7. I initiate and develop SOPs standard operating procedures and enforcement to staff.
8. I carry regular safe inspections to check and ensure that policies and procedures are properly maintained
.9. Production process monitoring in compliance with CGMP, development of SOP and application of TQM in manufacturing of products.
10.I train all categories of staff in CGMP,HSE and facilitate in- house workshop.
I have a practical experience in management of all categories of waste to reduce cost.
I treat all source of microbial contaminant in water systems to ensure compliance to water quality.