?Company Overview:?? ?Elanco is a global research-based company that develops and delivers product and services to enhance animal health and production. We value innovation, both in scientific research and daily operations, and strive to cultivate a collaborative work environment for more than 7,000 employees worldwide. Founded in 1954, Elanco is a division of Lilly. Our worldwide headquarters and research facilities are in Greenfield, Indiana.Responsibilities:Commercial ManufacturingProvide technical support to contract manufacturersDevelop and maintain manufacturing instructions for EEM governed productsWork with cross-functional groups to troubleshoot issues arising at CM sites, including but not limited to deviationsMaintain an appropriate presence during manufacturingReview process and product data for adverse trends; assess and understand process capabilityServe as primary technical resource for manufacturing process.Identify, evaluate, and implement process improvements with a focus on capability, compliance, and cost.Conduct / support process validationAuthor Annual Product ReviewsNew Product Commercialization- Activities as needed/requested by TS/MS Commercialization GroupParticipate in the evaluation of new business opportunities thru due diligence, product reviews, and cost modelingSupport the commercialization of new products by partnering with TS/MS Commercialization or R&D colleagues throughout the development processEnsure manufacturing concerns are addressed at phase-appropriate points of development; effectively apply principles of QbDFacilitate the Manufacturability Review processSupport the identification, selection, and approval of contract manufacturersLead technical transfer, process implementation, and validation activitiesSupport launches in secondary markets, ensuring regulatory commitments are aligned with process capabilitiesBasic Qualifications:?? ?Bachelors of Science Degree (Engineering, Chemistry, Biology, Pharmacy) .1 year experience in manufacturing and/or development of Pre-mix productsQualified candidates must be legally authorized to be employed in the United States. Lilly does not anticipate providing sponsorship for employment visa status (e.g., H-1B or TN status) for this employment position.Additional Skills/Preferences:Understanding of cGMP requirements for drug substance and drug product manufacturingStrong problem solving skills, including strategic and creative thinkingStrong interpersonal skillsClear, concise communication skills (both written and verbal)Cross-functional networking skills: demonstrated ability to influence othersStrong analytical skillsAbility to handle multiple priorities and deal with ambiguityComputer literacyDemonstrated ability to achieve results with peopleProduct commercialization experienceUnderstanding of or experience in multiple technology platforms (small molecule, large molecule, oral solid dose, liquid formulations, etc)Understanding of additional regulatory requirements (e.g., EPA, USDA)Knowledge of statistical methods and applicable softwareUnderstanding of analytical methodsWorking knowledge of RegulusWorking knowledge of TrackwiseAdditional Information:?? ?Approximately 10-25% travel to contract manufacturing sites, primarily within North AmericaLilly is an EEO/Affirmative Action Employer and does not discriminate on the basis of age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability or any other legally protected status.?Removal Date: 02-Feb-2017Apply for this job.