Ecem Dogan Email & Phone Number

Stockholm County, Sweden

Stockholm County, Sweden

Sweden

İstanbul, Türkiye

Responsible for the management of material master data throughout the pharmaceutical material life cycle.• Ensure the accuracy, completeness, and consistency of master data across all SAP modules and systems.• Identifies gaps between the existing Master Data components and the required ones.• Generating Master Data reports to support key stakeholders within the business.• Develop and maintain SAP master data procedures and best practices.• Create and maintain SAP BOMs for pharmaceutical products, ensuring that they accurately reflect the product structure and components.• Create and maintain SAP PV data for pharmaceutical products, ensuring that all versions of the product are accurately maintained in the system.• Collaborate with cross-functional teams to ensure that SAP master data aligns with business requirements and process flows.• Train users and stakeholders on SAP master data management best practices and procedures.

Istanbul, Turkey

Working on SAP deployment project in Supply Chain Department involving all the stakeholders of Business• Ensures that all aspects of the project are on track and accomplished on time and schedule. • Lead the project and business teams through integration testing and UAT & BRT; and track test defects are resolved.• Collaborate with SMEs and global stakeholders & ensure the decision support.• Prepare timelines for the project and align with all the business stakeholders for accomplishments.• Providing training to all key users and end users by consultants and lead in house hyper care activities.• Responsible for managing the relationship with the local SMEs and relevant global stakeholders, planning meeting organizations to follow up issues.

İstanbul, Türkiye

• Creating monthly and quarterly Process Validation plans and organizing weekly validation meetings.• Writing Process Validation Protocols and Reports and conducting studies.• Ensures that the validation processes are carried out in accordance with the defined parameters, quality standards and production plan.• Performing validation MBR checks before validation studies.• Leading Cleaning Validation Weekly Meetings and follow up the weekly plan.• Performing CHT, DHT and BHT studies.• Being responsible for the PV and CV master plans.• Participating in data integrity studies and providing necessary personnel training in the department.• Action tracking on AQWA and Agile Systems.

Lisans Derecesi, Chemical Engineering

Master'S Degree, Çevre Bilimi

Yüksek Lisans (Master), Life Sciences, Erasmus