In this role, the selected candidate will be responsible for general and specific assignments involving complex and novel types of plans, investigations, surveys, environmental impact assessment, major regulatory issues, permits, approvals, comments, and expert testimony preparation and presentation.
In this role, you will be responsible for generation of both novel targets and new parasiticide interventions in companion and food animals, with strong technical emphasis in high content, medium to high throughput electrophysiology.
In this role, the candidate will identify scientific issues and solve problems, both individually and with partners from multiple therapeutic areas and functional groups (protein engineering, cellular biology, etc.).
In this role, the selected candidate will support the technical transfer process, investigations, and batch record generation for cGMP manufacturing and to partner with internal and external clients to design and support manufacturing processes.
In this role, the candidate will perform research and develop methodologies, especially in business analytics/data mining and other innovative statistical/mathematical approaches to solve business problems if necessary.
In this role, the selected candidate will perform facility fit evaluation, then technology transfer and scale up of Downstream protein manufacturing process in conjunction with the process development laboratory, client, manufacturing, and quality assurance.
In this role, the candidate will integrate pharmacokinetics and PK/PD with discovery biology to define structure activity relationships to guide protein engineering strategies and to help optimize development of protein therapeutics.
In this role, the selected candidate must have an experience communicating insights from complex data to non-technical audiences; experience in general programming language such as Ruby, Python, Perl, Java, or C.