Purification Lead - Pharmaceuticals

- As a scientist in the Purification Development group, you will identify and develop new purification technologies, work to design optimized downstream drug substance processes for new biologic candidates, employ strategic thinking to overcome technical hurdles and oversee process technical transfer to GMP manufacturing facilities, as they make their way from discovery to the clinic.

- All scientific work in development will occur in CROs and CMOs and the scientist has to work to identify gaps in them and work effectively to ensure high quality product and information is delivered back to Lilly. The scientist should have the technical ability to troubleshoot issues as they occur, and to identify trends and opportunities to reduce process variability, A strong scientific foundation is a prerequisite for this role.

- The role requires a lot of flexibility and adaptability in accepting new projects and challenges.

- In addition, the ability to exhibit a high level of attention to detail, a quality-minded approach to experimental design, and record keeping is essential. Maintaining accurate records and interpreting data to provide detailed information and analysis on the execution of experiments will be a daily activity.

- Writing technical reports, tech transfer documents and giving presentations to summarize development activities are important deliverables.

- This role requires effective interaction and communication of technical information with, but not limited to; Safety, Environmental and Quality Team members, Purification Development colleagues, CMC Team members, Discovery team members, Analytical Services, Tech Service/Manufacturing Science representatives, Operations, Engineering, Regulatory and Maintenance personnel.

- The scientist has to adhere to all safety and environmental guidelines and promote a proactive safety culture and environmental compliance in all areas.

Educational Requirements :

- PhD in Chemical Engineering focused on biological separation sciences with 3-6 years of relevant experience.

- 3+ years relevant experience in leading protein purification/process development Experience