Quality Assurance Manager
May 2012 — July 2015
Responsible for maintaining the following FDA quality system records current and up to date at all times according to FDA cosmetics act( The listed records below are the basis and focus of all FDA Inspections).
Master Batch Records, Production Batch Records, standard Operating Procedures, Standard Operating procedures, Employee Training Records, Supplier Qualification Records, Active Ingredient/Raw Material/Label Usage Reconciliation Records, Finished Goods Distribution Records, Internal GMP Audit Records and Customer Complaint Records.
Ensured that all systems are in compliance by conducting periodic self audits utilizing pre-set audit schedules and audit checklist.
Conducted monthly retain observation test of finished products
Maintained compliance calendar to submit renewals of licenses, permits ect. that are expiring in a timely manner.
Assist to process Export Certificates and Free Certificate of Sale.
Provided weekly status reports to Management.
Perform other assignments that may be directed by Management.