Work in a GLP or GMP environment with appropriate documentation and safety practices. Develop analytical strategies in support of pharmaceutical drug products during all development phases, including supporting manufacturing process development, developing, validating and transferring analytical methods, designing stability studies to understand drug degradation mechanisms and for shelf-life assignments, and developing impurity control strategies. Plan, direct, and review the lab work of other scientists in a matrix environment. Collaborate with colleagues to identify appropriate analytical approaches, including use of computational predictive tools, modeling software and data visualization tools where appropriate. Critically review and interpret scientific data to derive clear conclusions and provide direction for future work. Communicate results and conclusions through various media including presentations and technical reports. Evaluate new approaches and ways of working, e.g. working with outsourcing partners. Comfortable utilizing different instrumentation and/or analytical technologies and mentoring other scientists in use and interpretation of data generated by different analytical techniques. Author relevant sections of the quality modules of regulatory submissions.