Job Details

DescriptionAs an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees.Duties & ResponsibilitiesResponsible for design management for MBR design activities at each site related to deployment of MES to all production departmentsResponsible for MBR design activities include records for deployment to new production areas and may also support new launch/transfer of products into the deployed production areasManages and delivers projects and processes for Operations with quality which impact economic growth potential, reduce market risk and support site throughput outcomes and results to meet key performance indicatorsDirectly responsible for the expansion and development of MES across the organization in support of advancing and growing the businessLeads the creation and maintenance as needed of master recipes in SAP and master batch records in MESProvides guidance for both PES and other Production related to best practicesServes as BIAH representative for the PAS X Regional User Group consisting of various pharmaceutical and vaccine manufacturers utilizing and integrating MESServes as SME in all ERP functionality related to PE regarding usage of SAP, SAP Master Recipes, MES and with understanding of related workstreams. The technicality of this role assumes local and global support activities when neededLeads and/or supports process improvement initiatives and project teamsLeads and mentors the lesser experienced team members with expertise to ensure appropriate documentation and procedures have been followed during the design processIncorporates process improvement methodologies (i.e. 5-step method for problem solving, six sigma, lean manufacturing, etc.) in working with project teamsIdentifies and formulates tactical solutions to assigned areas of focusResponsible for regularly coordinating and communicating with support functions such as Production Planning, Quality Assurance, Maintenance, Engineering or other cross functional areas in support of process improvement and other maintenance activities to meet requirements and timelinesResponsible for leading/managing multi-site CAPA implementation, auditing and revision of standard operating procedures for compliance related to MES processes and MBR creation and updatesResponsible for overseeing the regular coordination and communication with support functions such as Quality Assurance, Maintenance, Engineering or other cross functional areas in support of CAPA implementation and process/documentation improvement activitiesCreates, reviews, and updates OJT & MBR curricula and compliance requirementsAssists with planning, scheduling and performance of job task analysis of electronic record designersEnsures Regulatory Compliance regarding process order data and batch recordsAssists with regional change controls, BOM and planning recipe updates to ensure compliance and correct costing of productsPerforms other duties as requiredRequirementsBachelor's degree in a STEM field, Business or related area of focus with a minimum of eight (8) years' experience implementing MES activities, supporting production processes, and/or executing relevant functions in a cGMP manufacturing/operations environment or similar organization requiredORIn lieu of degree, a minimum of twelve (12) years' experience implementing MES activities, supporting production processes, and/or executing relevant functions in a cGMP manufacturing/operations environment or similar organization requiredMinimum of two (2) years' experience with PAS X or other MES related software requiredProven experience as a project manager including formal or informal leadership of project teamDemonstrated decision making, communication, planning and organizing abilitiesOrganizational change management experience is preferredRelevant industry experience must be inclusive of a strong, working knowledge of MES, ERP and applicable systemsMust be proficient in MS office applications including Project, Word, Excel, Outlook, etcDemonstrated knowledge of relevant production and/or packaging techniques and equipmentDemonstrated proficiency in applicable software applications utilized in production and/or packagingA working knowledge of cGMP, EU and OSHA guidelines as they pertain to implementing process improvements to production and/or packaging equipmentDemonstrated ability to train others and complete OJT/training assessmentsAbility to follow systematic continuous improvement methodologies and the willingness to identify, define and implement process improvementsTravel requirement of 30%Eligibility RequirementsMust be legally authorized to work in the United States without restrictionMust be willing to take a drug test and post-offer physical (if required)Must be 18 years of age or olderWhy Boehringer Ingelheim?With us, you can develop your own path in a company with a culture that knows our differences are our strengths - and break new ground in the drive to make millions of lives better.Here, your development is our priority. Supporting you to build a career as part of a workplace that is independent, authentic and bold, while tackling challenging work in a respectful and friendly environment where everyone is valued and welcomed.Alongside, you have access to programs and groups that ensure your health and wellbeing are looked after - as we make major investments to drive global accessibility to healthcare. By being part of a team that is constantly innovating, you'll be helping to transform lives for generations.Our CompanyWant to learn more? Visit