Head, Quality Improvement & Document Control

• May 2017 - Present

Senior Quality Assurance Analyst

• Nov 2015 - May 2017

Quality Assurance Analyst

• May 2011 - Nov 2015

•Ensure that all medicinal products manufactured in swipha are designed and developed in a way that takes account of the requirements of Good Manufacturing Practice (GMP) and Good Laboratory Practice (GLP).•Ensure that arrangements are made for the Manufacture, Supply and Use of Raw Material, Finished product and Packaging Material by establishing an SOP controlled system and documentation that gives evidence of all operation. •Ensure that all necessary controls on bulk and finished products and any other in-process controls are validated and governed by WHO compliant SOPs.•Ensure that Medicinal products are not sold or supplied before a qualified person has certified that each production batch has been produced and controlled in accordance with the requirements of the Marketing Authorization and any other regulations relevant to the production, control and release of Medicinal products. This is achieved by reviewing and approving all Batch Production and Packaging Records before distribution and sales of the product. •Put up a satisfactory arrangement system in place such that Medicinal products are stored, distributed and subsequently managed to ensure consistency throughout shelf life and to prevent mix up. •Put in place a Procedure for Self Inspection and or Suppliers Quality Audit which regularly appraises the effectiveness applicability and improvement of the Quality Management System.•Effective control and retrieval of all obsolete documents for archiving or destruction as is the case. •Review of all Good Manufacturing Practice Document (Batch Production and Packaging Records, Protocols, Reports, Certificate of Analysis e.t.c) with a view to establishing and maintaining a coding, numbering and indexing system within swipha, and to maintaining the WHO standards for documentation and archive.•Collation of data and writing report for Annual Product Review.•Handling of Product Complaints and Recalls. Show less

Intern

• Jun 2008 - Aug 2008