• A highly qualified laboratory scientist with 20 years of experience in FDA regulated laboratories in the Pharmaceutical and Biotechnology industries
• Strong auditing and laboratory skills with great attention to details (GLP)
• Versed with the 21 Code of Federal Regulations (CFR) 210, 211 and 820 for class two medical devices
• Used the United States Pharmacopoeia (USP/NF), the British Pharmacopoeia (BP), the French Pharmacopoeia (FP), the European Pharmacopoeia (EP), and the Merck Index
• Laboratory experience in the cGMP manufacture...