Job Description:
- Pay: 60.00-69.00/hr.
- Length of Assignment: 2 years to start with potential for extension or conversion.
- Hybrid role: onsite 3 times a week but can flexible.
- Travel reimbursed - not expecting much travel but here and there might be a tiny bit if at all.
- Must have technical experience with small molecule.
- Track progress of project, review data, write reports, review reports, provide feedback on technical and scientific aspects of the project.
- The overall scope of this position is to manage CMC development and Pharmaceutical Technical activities in support of new R&D compounds, Life Cycle Management Programs (LCM), product territory extensions and industrial technical projects.
- As a member of MSAT Synthetics and Oral Solids, you will be responsible for the coordination of multiple technical aspects of MSAT and Manufacturing and Supply (M&S) Programs through organization and alignment with other group divisions (Commercial Global Business Units, R&D, Regulatory, Alliance Management, etc.), various internal support laboratories, and contract CMO facilities.
- Specifically, you will be involved in pharmaceutical development activities (small molecules) for oral dosage forms such as tablets or suspensions. Additionally, as new products approach the registration / launch stage, you will work closely with MSAT CMC Leader, M&S Sites, Supply Chain, CMO’s (with External Manufacturing) and Alliance Partners to outline plans and activities.
- Executes 2nd generation program technical strategies to the MSAT Technical Product Team, focused on pharmaceutical development of oral dosage forms for small molecules.