Associate / Principal Scientist - Analytical Development The Large Molecule Technical Development organization of Elanco is hiring for a Principal Scientist to play an instrumental role in our organization! The Principal Scientist is a senior scientific role whose primary responsibility is to lead program-specific method development activities for therapeutic proteins in our company's biologics portfolio, from the discovery interface through first product registration. In this role, you will provide hands-on, day-to-day technical and strategic leadership and work closely with cross functional teams in Analytical Development, Process Development, Global Quality and Regulatory Affairs-CMC, and our partners in in the commercial/manufacturing to support commercialization of our company's large molecule products. The ideal candidate will have knowledge in the development of biologics, including monoclonal antibodies and complex protein modalities. Research and industry experience should demonstrate successful application and management of state-of-the-art analytical techniques to solve problems, including strong background and experience in separations science and extensive experience with UPLC/HPLC analysis of biologics (e.g. SEC, RP, IEX). Experience in microbiological techniques, ELISA, PCR and cell-based analytics is preferred. We are looking for a team player with strong leadership skills and the passion for mentoring and working along others in a laboratory setting. Applicants must have effective organizational and multi-tasking skills, have demonstrated excellent scientific leadership, and have superior communications skills, both written and oral. A track record of delivering impactful solutions to complex problems, and evidence of strong cross-functional collaboration is expected. Experience leading small groups of technical personnel, leading projects, and defining group or departmental strategy will aid in distinguishing candidates. Job Responsibilities: • Extensive experience in analysis of biologics (e.g., Size Exclusion Chromatography (SEC), Ion Exchange Chromatography (IEX) RP-HPLC and affinity chromatography. • Strong background in electrophoretic methods like cIEF and capillary electrophoresis along with LC/MS methods • Strong background in analytical control strategy development and execution • Demonstrated ability to develop talent through good mentoring skills • Demonstrated ability for taking initiative, creativity, and innovation in problem solving • Background in Analytical Methodologies and sound scientific understanding of Critical Quality Attributes/QbD/DOE principles as well as data analysis and statistics for setting specifications • Ability to design, execute and/or direct the development and qualification of release, characterization, and stability assays for testing of clinical trial material and in support of product and process development • A strong team player with excellent oral and written communication skills; ability to work both independently for development of assays and cross-functionally for successful transfer of assays; Plan assay optimization and documentation to meet program deadlines • Authoring and reviewing internal technical reports, sections of regulatory filings and external scientific publications • Experience with matrix management and peer to peer coaching • Strong ability to deliver complex objectives under aggressive timelines in a rapidly changing environment. Basic Minimum Qualifications: • Ph.D. in analytical chemistry/biochemistry or related field with a minimum of 8 years of experience in the pharmaceutical industry, M.S. in analytical chemistry/biochemistry or related field with a minimum of 12 years of experience in the pharmaceutical industry, or B.S. in analytical chemistry/biochemistry or related field with a minimum of 16 years of experience in the pharmaceutical industry. Preferred Experience and Skills: • Experience with qualification, validation, and transfer of assays to a GLP or regulated laboratory environment as listed in ICH Q2 and USP • Knowledge and experience with structure-function assays and link to mechanisms of actions • Understanding of protein degradation mechanisms and link between analytical methodologies for analysis • Experience with complex glycan analysis • Experience in analysis of various Biologic modalities (e.g., mAb, antibody-drug conjugate, fusion protein). • Established scientific reputation supported by publications and external presentations • Strong interpersonal skills. Demonstrated ability to collaborate with and influence teams Additional Information • Location: Global Elanco Headquarters - Greenfield, IN (NEW HEADQUARTERS COMING Q1 INDIANAPOLIS, IN) Don't meet every single requirement? Studies have shown underrepresented groups are less likely to apply to jobs unless they meet every single qualification. At Elanco we are dedicated to building a diverse and inclusive work environment. If you think you might be a good fit for a role but don't necessarily meet every requirement, we encourage you to apply. You may be the right candidate for this role or other roles! Elanco Benefits and Perks: We offer a comprehensive benefits package focusing on financial, physical, and mental well-being while encouraging our employees to pursue our purpose! Some highlights include: • Multiple relocation packages • Two weeklong shutdowns (mid-summer and year-end) in the US (in addition to PTO) • 8-week parental leave • 9 Employee Resource Groups • Annual bonus offering • Flexible work arrangements • Up to 6% 401K matching