Global Process Automation Software integration Expert

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. What You’ll Be Doing The overall Global Parenteral Program (GPP) team is made up of a cross-functional group embedded in their respective functions. The goal of GPP is to: 1) align Manufacturing processes to a single Operational Control Strategy across the Parenteral and Device Assembly and Pkg network, 2) maintain the alignment of the new platforms throughout their life-cycle in an integrated fashion, 3) support the alignment of key operational practices and key business processes based on prioritization defined by owning functions, 4) integrate Network cross-functional agendas, and 5) manage an effective Parenteral/DAP Network knowledge Management process. The position will be responsible to work with local automation project teams and global teams responsible for Global Manufacturing Systems (MES, EWM, ATTP, Robotics) to standardize solutions to accelerate delivery of new parenteral cartridge lines. This position will report to a Director in Tech@Lilly – MQ. How You’ll Succeed Must bring technical knowledge and experience to influence and harmonize process automation and integration solutions across all the parenteral cartridge lines and formulation work centers working with global teams.Must support the integration of the Parenteral network with the Tech@Lilly – MQ global Functional agenda (and vice-versa).Must assure Data Integrity management according to Lilly Policies.Must lead improvement, maintenance, and LCM of existing integration layer for Cartridge platform.Must facilitate the effort to replicate technology solutions and harmonization of common business processes within the cartridge program.Must provide centralized management of validation activities in alignment with Lilly CSV policies for systems in the DAP Integration Layer, including incidents and changes in Service Now.Must be able to work across organizational boundaries to ensure alignment and leverage enterprise patterns and services. What You Should Bring Ability to replicate technology solutions and harmonization of common business processes in a global environment.Broad and deep technical knowledge and experience across varying automation software platforms.Experience with providing technical guidance to other members of the organization, including developers, project managers, and technical support staff.Excellent communication and interpersonal skills to build relationships with stakeholders and articulate complex technical concepts.Analytical and problem-solving skills to identify and resolve complex technical issues.Adaptability and flexibility to work in a fast-paced, dynamic environment and manage multiple tasks simultaneously.Experience with Computer System Validation, data integrity, batch review by exception.Demonstrated knowledge about cybersecurity topics in Manufacturing environment.Demonstrated knowledge about Manufacturing S95 network and how different layers are utilized by ITOT systems.Working knowledge of Cloud Technologies and demonstrated desire to learn more about new technologies to help further manufacturing digital agenda.Bachelor’s degree in or higher in IT related field, engineering, or automation. Your Basic Qualifications Deep knowledge in automation.At least 5 years of experience in automation in manufacturing or manufacturing related areas with most of that experience in pharmaceutical manufacturing.Demonstrated ability to learn and apply technical knowledge in manufacturing operations.Fluent English. Additional Skills/Preference Ability to work in a multi-cultural environment.Prior experience in IT projects.Prior experience in global projects in Pharma. Additional Information Global Role – Must be resident at a Lilly baseload manufacturing site, preferably Fegersheim (near Strasbourg, France).Frequent travel will be required to other manufacturing sites and OEMs in US and/or Europe.Home office possible, up to 3 days per week. #J-18808-Ljbffr