- Charles River Laboratories (Mattawan, MI)
- …worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on ... **Job Summary** The Immunology and Immunochemistry disciplines support large molecule drug development using ligand binding assays (LBA), such as enzyme-linked… more
- Colorado State University (Fort Collins, CO)
- …RVT ), OR Provisional Veterinary Technician ( PVT ) through the Department of Regulatory Agencies with a clear plan including the timeline for obtaining full RVT or ... ( CACVT ) AND registered through the Department of Regulatory Agencies ( DORA ). Please visit the CACVT...and assist with catheter placements. + Accurately perform basic drug calculations. + Able to observe and recognize changes… more
- Cambrex High Point (Durham, NC)
- …a leading global contract development and manufacturing organization (CDMO) that provides drug substance, drug product, and analytical services across the entire ... analytical support, such as release and stability testing of drug substances and drug products. Able to...+ Responsible for ensuring compliance with cGMP and other regulatory guidelines. + Analyze information for technical correctness and… more
- Catholic Health Initiatives (Houston, TX)
- …infusion type medications including ancillary treatments; providing patient counseling and drug therapy monitoring to ensure patients receive safe, efficacious and ... accordance with protocols, internal guidelines/standards, and Board of Pharmacy regulatory requirements. **Position Responsibilities** + Provides pharmacy services and… more
- Charles River Laboratories (Shrewsbury, MA)
- …worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on ... management, interpretation and reporting of study data, and assuring the regulatory compliance of these projects. ESSENTIAL DUTIES AND RESPONSIBILITIES: Serve as… more
- Lilly (Indianapolis, IN)
- …maintain a state of continuous inspection readiness and full compliance with applicable regulatory guidelines, including ICH Q-series and 21 CFR Parts 11, 210, and ... through commercialization. + Align integrated development plans across key functions ( Drug Substance, Drug Product) and interfaces (device, discovery,… more
- Lilly (Indianapolis, IN)
- …Lilly and Company supports the design, development, and commercialization of drug products and pharmaceutical delivery systems including medical devices and ... and commercialization of medical devices and owns the development and qualification of drug substance (API) and drug product packaging components and container… more
- AbbVie (Irvine, CA)
- …and reporting of non-clinical data and communications/agreements with global regulatory agencies in the areas of Translational Pharmacology, Non-clinical ... therapeutic areas. The organization is responsible for defining the relationship between drug exposure (eg, concentrations in blood/ local tissue) and efficacy and… more
- Charles River Laboratories (Shrewsbury, MA)
- …worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on ... and assignments meet client needs. o Maintain the scientific, safety, and regulatory compliance integrity of the entire bioanalytical process. o Provide hands on… more
- Charles River Laboratories (Mattawan, MI)
- …worked together to assist in the discovery, development and safe manufacture of new drug therapies. When you join our family, you will have a significant impact on ... the evaluations of test compounds by providing bioanalytical quantitative analysis of drug in body fluids and tissues from non-regulated and regulated studies… more