Description:
Biotechnology Research,Commercial Physical Research,Biopharmaceutical Manufacturing,Upstream Process Development,Purification Process Development,Cell Line Development,Analytical Method Transfer,Analytical Method Development,Analytical Method Validation,Project Management,Regulatory Compliance,21 CFR 210 and 211 (Drugs),21 CFR 600,606,and 610 (Biologics),21 CFR 820 (Medical Devices),21 CFR 1270 and 1271 (Human Cells,Tissues and Cellular and Tissue-Based Products),ISO 9001 (General Quality Systems),ISO 13485 (Medical Devices),US Government Contracting Read More
