The chosen candidate will be responsible for process development, scale-up, technology transfer, establishing and optimizing commercial manufacturing processes for compounding and filling of solids, soft-chews, non-sterile liquids and sterile inject (aseptic manufacturing) platforms, as well as collaborating and partnering with Manufacturing, Engineering, and Quality organizations.
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, 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 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.
Assist with automated data processing and archiving, LIMS maintenance and customization, workarounds for unmet regulatory compliance issues with instrument software, professional level programming of custom software application needs, and re-implementing automated report generation.
In this role, you will develop and maintain interactions with Thought Leaders, appropriate HCPs, and access stakeholders, within a given geography to answer scientific, unsolicited product and HEOR related questions.
In this role, the selected candidate will coordinate new installations, including facility inspections, instrument validation, and customer training; review and approve operational quality of equipment, and instruct customers in operations and maintenance of system under general instruction.