This scientist will develop formulations for oral solid dosage forms (tablets and capsules) on high-priority programs with accelerated timelines. Key responsibilities include designing and executing formulation and process development experiments, interpreting scientific data, and communicating findings to stakeholders. The role requires close coordination with cross-functional teams to meet tight project deliverables and authoring technical reports and CMC sections for regulatory submissions.Position Responsibilities:Understand project timelines and deliverables and plans/coordinates project work accordingly with stakeholders.Contribute significantly and independently to project work which may include multiple projects within functional area.Review, interpret and communicate data within project teams.  Plan and implement resolutions to technical problems/issues.Independently design and execute experiments and report results.Proactively analyze manufacturing issues and coordinate potential resolution with the drug substance team.
