Plasma Classification Sr. Inspector
GrifolsAbout the role
Would you like to join an international team working to improve the future of healthcare? Do you want to enhance the lives of millions of people? Grifols is a global healthcare company that since 1909 has been working to improve the health and well-being of people around the world. We are leaders in plasma-derived medicines and transfusion medicine and develop, produce and market innovative medicines, solutions and services in more than 110 countries and regions.
Plasma Classification Senior Inspector
Summary:
This position requires a full understanding and knowledge of the Plasma Classification department which includes Master Schedule shipping and target dates and clear understanding of Industry and compliance to operating standards. The right person for this job will have full knowledge of the Classification databases to logically reason and use problem-solving skills to work through problems and find solutions. Further responsibilities may include startup and shut down of the Automatic Conveyor system and expediting the day’s work schedule. The position further requires handling and processing unsuitable plasma units per disposition order. Employee must be able to reconciliation of all units processed by using the Plasma Management System (SGP).
Responsibilities:
1. Working knowledge of Production Unit (PU) processing steps using the Plasma Management System (SGP).
2. Responsible for scanning and inventorying of plasma units assigned to a production unit (PU) utilizing a barcode reader.
3. Responsible for identifying and removing units according to various rejection criteria found during visual inspection.
4. Responsible for disposition, classification, and processing of unsuitable plasma units that are marked for removal during any step of the plasma process
5. Responsible for identifying and blocking units from further production when units fail to meet customer requirements.
6. Responsible for identifying unreleased units and transferring those units into sub shipments during the PU process
7. Responsible for verification of sub-shipment identification and location at the end of the PU process.
8. Responsible for identifying and entering abnormalities into SGP via the “Statistics” function, during or after the PU process
9. Responsible for completing the partial case between PUs
10. Responsible for clearing the production line of all material processed in a completed PU before starting the next PU process.
11. Responsible for transferring units between PUs and from a LOT to a PU.
12. Responsible for the scanning of case/units to a 3rd party sale utilizing the Disposition Module in SGP
13. Responsible for the scanning of case/units for a Material Destruction Order (MDO) utilizing the Disposition Module in SGP
14. Responsible for scanning of archive sample vials assigned to a Sample Archive (SA) utilizing a barcode reader.
15. Responsible for ensuring plasma does not exceed the allowable time out of freezer during production, utilizing the SGP warning system.
16. Able to maintain record accountability and demonstrate accuracy
17. Responsible to reprint labels as necessary from SGP
18. Responsible for using reporting database to print all necessary paperwork to facilitate the beginning of work on a PU
19. Working knowledge of Human Machine Interface (HMI) to set stacking patterns for different types of plasma cases
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