A BSc in Biological science, biotechnology or related field with 4+ years of relevant assay development and industry experience. Drive, design and lead assay development, validation and optimization of a variety of biochemical and cell based assays.

The Translational Medicine (TM) team is seeking a highly motivated Scientist I to lead the development of target engagement, pharmacodynamic and biomarker assays, in the context of drug development across the Horizon pipeline and a variety of therapeutic areas.

Manage CROs to establish assay development, assay validation and assay transfer for biomarkers to appropriate regulatory standards. Track record of successful design, optimization and execution of assays for drug development.

INL/GPP is responsible for working with various counterparts across the Department of State and within the U.S. interagency, including the Department of Justice, the Drug Enforcement Administration, the Department of Homeland Security, U.S. Customs and Border Protection, and the Department of The Treasury.

Prior experience with pre-clinical or clinical drug development teams is preferred. Strong understanding of the drug development process. The candidate will be responsible for the design, development, optimization, validation and execution of assays, as well as interacting with and managing vendors and contract research organizations (CROs.

Represent NRWS on cross-functional teams, and will lead the nonclinical submission sub-teams, working in close partnership with Global Regulatory Affairs (GRA) and nonclinical subject matter experts (SMEs) from pharmacology, drug metabolism and pharmacokinetics (DMPK), drug safety research and evaluation (DSRE) functions and external collaborators.

Familiarity with quantitative systems pharmacology and other applications of modeling and simulation within pharmaceutical drug discovery and development. Integrate diverse data sources, such as in vitro cell culture, immunoassays, clinical measurement, and/or large-scale genomic and transcriptomic assays, into model development and calibration workflows.

Provide technical advise on new or modified practices, methods, and techniques for relevant DoD training exercises Provide leadership and technical support to the design, development, and implementation of USAID designed exercises.

Senior Scientist - Downstream Process Development. As a condition of employment with PPD, part of Thermo Fisher Scientific, in this role, you must have received your Covid-19 vaccine and you must disclose proof of your vaccination status upon employment.

Previous experience in an analytical development department working in the field of vaccine development. Apply knowledge in drug delivery systems and corresponding analytics to improve and support product and process development of vaccines.

Work with Creative Director and Executive Chef to determine development calendar and internally promote new items. Collaborates with Culinary Admin Team and Purchasing Manager to build out recipes, source and price verify for newly developed items to meet both development and budget requirements.

Establish close working relationships with other Director level leaders in the areas of SAIS Europe, Corporate and Foundation Relations, Constituent Engagement and Alumni Relations, and with central JHU Development and Alumni Relations colleagues including Annual Giving, Gift Planning, and Prospect Research, to ensure that the Major Gifts Team is well-coordinated with the rest of the fundraising enterprise.

Work independently, or with little guidance, to evaluate, develop, and validate HPLC procedures or other methodologies for the analysis of identification, assay and organic impurities for small molecule drug substances, drug products, dietary supplements, food ingredients and excipients.

The PNNL's Buildings Simulation & Design Group provides energy simulation, tool development, and workflow automation for energy policy impact analyses and integrative building design processes.

The Associate Program Management Director/Senior Program Manager will drive the program teams forward in the development of novel antibody-based therapeutics within our oncology portfolio. Eight (8) years of relevant work experience in life sciences (eg biotechnology or pharmaceutical industry, research laboratories, contract research organizations), preferably with experience in drug development and oncology, including prior management of preclinical/research focused development efforts.