Havertown, PA, 19083
... SOPs Streamlined continuous improvement processes and program management which generated improved KPIs, financial metrics Met FDA deadlines for Alkermes safety updates by working closely with internal Medical Legal Review process Team Lead National ...
- May 01
Powder Springs, GA
... terminology • CGMP • Hand tools • Electric pallet jack • Warehouse experience • Order picking • Hotel experience • Sanitation • FDA regulations • Computer literacy • Kitchen experience • Packaging • Logistics Certifications and Licenses Food Handler ...
- May 01
Montville, NJ
... and site assessment Individual and large group training on EDC methods and best practices Liaison between sponsors, the FDA and research sites Responsibilities included a Phase III dermatology NDA, a pre-market maintenance study for a new ...
- Apr 30
Diamond Bar, CA
... Deepened relationships with key vendors / suppliers and department heads, provided empowering leadership to employees, audited, and monitored KPIs and Compliance (DOT, FDA, GMP, GWP, OSHA, etc.) Crocs, Inc. (NASDAQ: CROX), Ontario, CA 2014 to 2016 ...
- Apr 30
United States
... • Phlebotomy • Specimen collection / processing • Acute care • Organizational skills • FDA regulations • Time management • HIPAA Certifications and Licenses AED Certification First Aid Certification CPR Certification PBT (ASCP) ASCP Certification
- Apr 30
Nesbit, MS
... Report to Medication Usage System Team • Analyze medication system variances, adverse drug reactions, and sentinel events along with FDA / MedWatch Alerts and ISMP findings and recommendations • Forward data and evidence to FDA • Community Awareness ...
- Apr 30
Brandon, FL
... total solids, viscosity, and Karl Fischer on hundreds of various products • Performed validations in accordance with cGMP, FDA, and Standard Operating Procedures, as well as USP methods • Completed documentation needed to support testing procedures ...
- Apr 30
Bellevue, NE
... a new Hepatitis A biochemical immunoassay, through discovery, research and development, clinical trials, data analysis, FDA submission and market entry in an aggressive timeline and time-sensitive environment Resolution of product deficiencies ...
- Apr 30
Lewis Center, OH, 43035
... • Additional experience in generating ANDA documents with FDA guidelines with more focus on CMC. • Familiarity with the drug and medical device development process. • Strong knowledge and understanding of ICH guidelines, cGMP, GLP, GCP, IND, NDA ...
- Apr 30
Silver Spring, MD
... Jan 2021 – Jan 2023 Visiting Scientist National Centre of Toxicological Research, FDA, Jefferson, AR • Accomplished flow cytometric analysis of anti-SARS-CoV antibodies in human plasma • Achieved protein linking to aldehyde/sulfate latex beads and ...
- Apr 30