Lamia Elneil's Linkedin Analytics

• Over 22 years of experience in the Dietary Supplement, Contract Manufacturing industry. Managed to bring the company to full compliance to the new 21 CFR 111 (Dietary Supplement cGMP). Through position as Director of Quality, established new quality systems that meet the FDA requirements such as Vendor Qualification, and equipment sanitation programs. Updated the company Standard Operating Procedures (SOPs), Training Program, and other quality systems. Proven track record in improving the Nonconformance quality system that resulted in reducing the product rejects by more than 50%. • As a Director of Quality for Contract Manufacturing plant, was responsible for meeting the requirements of more than one hundred active domestic and international customers. Managed to qualify over 3,000 raw materials from more than 50 suppliers. Supervised the R&D unit and approved the new product formulation for tablets, capsules, and powder drinks dosage for domestic and international markets. Managed product stability program for international customers. • Managed the Quality department staff and annual budget of $250,000. • Evaluated our Customer Labels to ensure compliance with the requirements of DSHEA (Dietary Supplement Health and Education Act), FTC (Federal Trade Commission), and any other regulatory agents.