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...