Agnieszka Borgoń

* Leading some Quality Projects mainly influencing on Technician's time reduction
* Being a coach in daily Quality Engineer's/ Technician's SAP issues. Sharing gained SAP Quality knowledge and experience
* Being a local area contact if needed of any Plant knowledge for BPS team
* Cooperation with EMEA team on added some options facilitating everyday Quality work
* Daily monitoring and resolving Quality queues
* Being a part of a success of Gate 7 BT and relevant tasks Completed. Working on completion tasks to Gate 8
* Leading solutions, improvements, implementation of new designs and functionalities
* Being a key support in repairing issues such as consequence of SAP Orange Code
* Taken part in defining Quality steps within Quality Material Extension Process
* Playing a key role in preparation of New Superuser implementation plan

Within Quality Engineer role I was delegated to Quality SAP Superuser to take part in SAP system impementation.

Responsibilities:

* Delivering all assigned project activities on time by completing it in full according to project's timeline
* Playing active role in SU network by sharing knowledge and experience. Be first point of contact for end users. Train all users according to the training plan
* Playing active role in MDM deployment activities
* Participating in regional / global meetings dedicated to respected area
* Performing data cleansing according to timeline
* Providing input for necessary documents
* Participating in MOCK, PIT testing
* Testing loaded data and creating defects using ALMQC if is needed

* Quality SAP implementation for all Industrial Adhesive Tapes Division area :
- implemented all required Control Plans for Process and Quality control
- implemented Control Plans for all controlled Raw Materials (Input control)
- implemened of Automatic Usage Decision for materials releasing from conditioning time
- implemented Certificates module (CoC, CoLC, CoA)
- taken part in Quality Notification implementation
- a big cooperation with Global Approvers to load correct settings for Batch Manage and shelf life
- implemented of Automatic Batch strategies depends on areas and requirements (ECC or MES Batch strategy creation)

* Responsible for coordination complaints from the customer (coordinating CFR base in Lotus Notes)
* Responsible for coordination internal, process and product audits in Poland Audit Center base in Lotus Notes
* Responsibile for coordination CAPA (Corrective Action, Preventive Action)
* Responsible for creation presentation for Management and calculating quality factors (for example: CCRT, PRT, DPPM)
* Responsibile from quality side for coating and converting area for adhesive transfer tapes (for example: customers complaints analysis, control of nonconforming product, to be a member of PPU process, taking part in NPI changes)

• 1st semester: Planner in Medical Site, leader in the project: Delivery advice in the MP and SCO warehouses;
• 2nd semester: Quality Engineer in 3M Aerospace Aircraft Maint Division, leader in the project: Productivity and handling improvement of autoclaving process at AAMD QC Laboratory;
• 3rd semester: Quality Engineer in 3M Personal Safety Division, leader in the project: To establish shelf lifes and storage conditions for raw materials in incoming inspection process.

• high performance liquid chromatography (HPLC) method;
• gas chromatography (GC) and gas chromatography with head space methods;
• IR transmission and reflectance methods;
• principles of Good Manufacturing Practice (GMP).

• providing various forms of prescription medicines;
• participating in the implementation of the prescription;
• checking prescriptions in terms of dose rates, if any non - compliance;
• orienting in Polish Pharmaceutics Index
(Farmakopea Polska VI).

• galenic preparations made according to the current Pharmacopoeia;
• principles of prescribing medicine;
• preparing dilution;
• checking prescriptions in terms of dose rates and any noncompliance.

• calibrating of the pH - meter;
• determinating proteins by the biuret method;
• manufacturing of pharmaceutical technology active substances;
• managing documents kept in the laboratory.