Senior Data Custodian - Material Master

Job Description CSL Behring, a leading global biopharmaceutical company, is looking for a full-time Senior Data Custodian. This position will lead the Life Cycle Management of key global (Master) Data across the enterprise using the Enterprise Master Data Governance tool (SAP MDG) and SAP S/4 HANA. This position will primarily own the following Data Domain(s) and related business data operations with the utilization of Master Data Governance (MDG) Standards and Procedures and SAP S/4 HANA: Customer Master Vendor Master And may also lead the other domains as a secondary job duty: Material Master Key Responsibilities: Data Maintenance/ Data Life Cycle Management Lead the maintenance of global Master Data, while ensuring that proposed additions, changes, deactivate requests etc. comply with Global data & governance standards, rules and policies. Lead and guide the Data Maintenance activities the supply chain operations group conduct such as Create/Change/Activate/Delete/Deactivate/Mass Change master data object Participate in Data Life Cycle Management activities such as: Data Quality audits Data cleansing  Data enrichment Etc. Operations / Support Responsible for the ongoing data operations of Master Data as it triggers various business applications such as SAP, LIMS, COMPANION, MII etc. Responsible for the regional and site specific data operations, change management, and maintenance of documentation. Responsible for maintaining proactive communication with respect to ongoing & completed master data create/change/delete change requests. Effectively executes master data change requests using workflow logs and ensures timely completion of review/approval/rejection by following SLA guidelines. Effectively executes the workflow to make sure changes made to the data successfully replicates to the ERP System (SAP S/4 HANA) Report the replication failures to corresponding technical support and as well as the initiator of the change request. Enforce data governance standards across global master data domain(s). Analyzes problems and escalates issues when needed to appropriate levels of BT (IT) or Business. Analyze, evaluate and optimize local and global complex business processes, multi-layered data structures and business applications to identify improvement potentials. Develop solutions and recommendations for critical process deviations in collaboration with the affected areas. Lead complex multi-site projects to establish global standards by representing the local site in global committees to establish global standards. Participate in group, cross-departmental and global business performance improvement projects. Shall exhibit broader knowledge of pharmaceutical business process to supportmaster data domain(s) Shall exhibit formal or informal responsibility of reviewing the appliance of data quality standards/rules/checksbefore activating/rejecting a master data change request. Shall be able to collaborate and communicate with Global Data Leads or Process Leads as and when required to mitigate or remediate issues relevant to data Shall be willing to learn and accommodate new business process (if any). Project Work Assumes project responsibilities as assigned for projects related to (potential) changes to Master Data Organize and align the actions necessary to lead a project for creating process flows, data cleanup or enrichment in terms of data cleanup or enrichment. Testing and Validation In the event of a project or upgrade, provide required assistance to BT(IT) teams in creating test cases and scripts that are relevant to the design and functional requirements while adhering to CSL defined quality and governance standards and procedures. Active participation in User Acceptance Testing (UAT) with Process Owners/Business stakeholders to ensure test applicability. Training Create regional or site specific SOPs, with a potential to global level. Lead the training activities related to Enterprise Data Management and maintenance. SOPs and Continuous Improvement Create/follow SOPs and work instructions etc. and for continuous improvement of the internal team processes based upon leading practices, evolving industry trends, expanding operational capabilities etc. Maintain Regulatory Compliance Effectively follows global BT (IT) procedures including the Quality Management System (QMS). Follows the appropriate global regulatory guidelines and current Good Manufacturing Practice (cGMP). Qualifications:   Required Skills & Experience: Bachelor's degree or equivalent experience; educational concentration in a computer-based or business administration discipline (e.g. Computer Science, Information Systems) or a technical discipline (e.g. Engineering, Mathematics) is preferred. 5+ years of experienceworking with a Data Management function Operational Experience with an enterprise Data Management tool (such as SAP MDG & SAP S/4 HANA) or any of the technologies Experience with Microsoft Office products, such as, Excel, PowerPoint, Access, SharePoint, Visio and Project Skilled Data handling and manipulation Preferred Skills & Experience (not required): Experience within the Master Data Domain Pharma/Biotech or similarly regulated environment experience Some knowledge of the Systems Development Life Cycle (SDLC) R-071783
Salary Range: NA
Minimum Qualification
5 - 7 years

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