Global Master Data Specialist

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.

POSITION SUMMARY

 

Responsible for the implementation of SAP related activities, including ongoing support within the Quality Systems Applications and Data Analysis group.  This role requires proficiency in the analysis of solution design, project implementation and master data accuracy to support the Supply Chain Planning activities for Grifols Biologicals.  Desired experience includes technical, functional and process expertise to drive strategic results for projects and initiatives within the Grifols organization.

 

 

ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned.

 

1. Ensure Master Data accuracy in SAP under a quality driven environment, involving raw materials, manufactured products and finished goods in line with corporate data standards. 
2. Work collectively under a team driven environment to update requirements in SAP for Production Planning, Materials Management and Facilities.  Strong emphasis in Segmentation, Serialization, Environmental Monitoring, Validation, Stability, Workflows and Notifications from SAP.
3. Provides support to quality operations and quality control with the daily activities required in order to achieve lot release targets for finished goods.
4. Perform duties related to processing and administering requests for data cleansing and standardization, identify areas of operational improvement by utilizing system functionality.  Including metrics and report design.  
5. Maintain current knowledge of regulatory and industry standards.
6. Generate thorough written reports, when required, that summarize investigations performed for out-of-specification results or out-of-procedure events.
7. Participate in regulatory and internal inspections/audits including providing written responses as applicable for area of responsibility.
8. Strict adherence to procedures and practices according to FDA regulations.
9. Strong emphasis on documentation according to FDA regulations.
10. Adhere to departmental corporate safety policies.

 

 

REQUIRED EXPERIENCE/SKILLS & EDUCATIONAL QUALIFICATIONS

 

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skill, and/or ability required. Reasonable accommodations may be made to enable qualified individuals with disabilities to perform the essential functions.

 

1. Bachelor’s degree in Business Administration, Operations Management, Material Science, Chemistry, Chemical Engineering, Computer Science or related scientific/ technical field is required. 
2. Related experience with ERP and APS systems in a pharmaceutical, GMP, or FDA regulated environment is preferred.
3. In depth understanding of the fundamentals of service end modules in SAP is required.  Relational database knowledge is preferred with platforms such as SAP, SQL and MS Access.
4. In depth understanding of customer-focused support influenced by manufacturing requirements for handling Production Planning, Quality Management and Preventive Maintenance master Data, understanding how master data supports transactional processes and integration for production.