Anna Żebrowska Email & Phone Number

Warszawa, Woj. Mazowieckie, Polska

Lead the engineering and quality implementation/industrialization of new products, as well as improvement of existing range to secure quality and compliance to all IKEA requirements.

Garwolin

Work with Global and Regional Marketing, R&D, Sourcing and Production teams to actively plan and support the introduction of new products to Manufacturing; Represent the department as a core team member to provide technical expertise for appropriate production process, material definition and overall design for manufacturability for new launches; Advise and Instruct Contract Manufacturers on Product Specifications, BOM’s and Quality requirements

Garwolin / Warsaw

Identify & track the project deliverables including customer and internal requirements; Create and deliver project work plans and revise them as appropriate to meet changing business needs and requirements; Measure and monitor supplier quality performance on an ongoing basis by managing Quality Operating System

Garwolin

Ensuring availability of components on time and in full for production according to a fixed production plan; Expedite and reschedule open purchase orders to suit production planning requirements; Review supplier capacity planning to ensure capacity requirements are satisfied based on sales forecasts; Build professional supplier and internal relationships in order to improve cooperation; Measure suppliers KPI’s and challenge them for continuous Supply Chain improvement

Garwolin

Support Project Co-ordination Manager in synchronization of activities (in Civil works, Processing and Packaging area) linked with the project realization, in order to ensure timely completion of project; Support in creation and update of the Rainbow project schedule to ensure clarity in understanding of the Project status and its next steps; Maintain efficient communication within the project team and business partners to assure required alignment of project tasks

Newbridge, Ireland

Completion of all processing documentation in accordance with current GMP and FDA regulations; Manufacturing of clinical trials, registration and validation batches on the GEA Pharma Systems and iFix application software; Setting-up, cleaning and operating production machinery and equipment; Completing paperwork for setting-up of a production order and inputting the paperwork to SAP System; Measure and monitor the moisture content of granulate; Performing in-process sampling and quality checks of Bulk Tablets in Processing Department; Sampling of purified water in production plant; Assisting maintenance in trouble-shooting issues