• Leading MDM Services organisation (25+) in GBS Center Network• Directing global master data and reference data processes and services• Driving BI data strategy in cooperation with global departments• Defining people development and leadership strategy in GBS along with senior leadership team from Germany, Argentina, Philippines, Poland• Leading data integration of product portfolio of BI’s biggest production plants and markets (US and France)

• Led a team of 9 experts responsible for approval of pharmaceutical materials for the entire company portfolio and material user support• Defined processes for maintenance and support in product and material domains• Led services and user support for domains product, material, reference data in multiple databases

• Led a team of 6 experts responsible for approval of pharmaceutical materials for the entire company product portfolio• Defining product data management processes• Coordinated global ERP implementation projects with focus on pharmaceutical materials (Mexico, China, Australia, New Zealand, UK, Italy, India, SEASK, CAMCAR, Spain, Greece)• Providing services and user support for product domain in multiple databases

Appointed to Project Lead of MDM workstream in SAP Implementation Projects given the experience in data migration, working with different SAP modules, and participation in previous SAP Implementation Projects.• Responsible for migration of material master for PTC Organization: data collection, analysis, and maintenance• Collaborates with Quality and Regulatory Departments on data collection• Communicates with the stakeholders, implements change management, provides training

Promoted to a position of increasing responsibility and complexity due to strong pharmaceutical background and knowledge about the system and business requirements. Performing a role of Global MDM Approver in SAP MDG workflow. Verifying and maintaining of pharmaceutical lists of values (LoVs) according to the global standard in cooperation with Global Pipeline. • Performed Global MDM Approval step in SAP MDG: assuring data completeness and consistency• Supported Material Harmonization Project in data collection and validation, communication with the stakeholders• Problem resolving in ServiceNow ticketing tool• Customer support in business matters• Maintained pharmaceutical LoVs in SAP MDG and Oracle• Co-author of Working Instructions for Global MDM Approval• Established new process for requesting pharmaceutical LOVs according to the global standards• Performed SAP MDG and SAP ECC system testing• Run material reports and mass uploads in SAP MDG• Provided user training for new staff members (2016)

Appointed to perform data allocation in SAP N20 and CataLogic, check the data with respective sources and regulatory databases. Responsible for SAP rollout in European countries. • Responsible for communication with respective stakeholders, data collection and validation in regular processes and in SAP Implementation Projects• Provided customer support and training on documents workflow and processes• Responsible for material master of SAP N20 Implementation Project for Estonia, Latvia, and Lithuania (2014/2015)• Responsible for material master of SAP N20 Implementation Project for financial hub in Switzerland (2015)• Worked with regulatory databases (e.g. Global InSight)• Performed data cleansing projects: check for missing and incorrect values, data collection and verification

Ward pharmacy, clinical trials, pharmaceutical logistics, writing guidelines for drug use, preparation of sterile and non-sterile medicinal products, compounding of parenteral nutrition admixtures, preparation of ready-to-administer antineoplastic drugs, quality control