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.

At Grifols, we believe that diversity adds value to our business, our teams, and our culture. We are committed to equal employment opportunities that foster an inclusive environment.

POSITION SUMMARY:

Reporting directly to the EQMS &QSAP Supervisor in Grifols Worldwide Operations (GWWO). The EQMS &QSAP Specialist will be required to complete and support activities within the Quality Department relating to SAP in Grifols Worldwide Operations Ltd (GWWO) for the site.

Key Responsibilities:

• Creation and maintenance of the Quality views for the material master data of all materials for procured, manufactured, and packaged materials/product

• Creation and maintenance of master data for inspection plans for testing of raw materials, semi-finished product, finished product and associated processes, including environmental monitoring, lab equipment, etc.

• Liaising closely with the Grifols sister sites in relation to the creation of master data for material/product transfer

• Creation and maintenance of Standard Operating Procedures for all tasks associated with SAP activities

• Compliance with procedures relating to GMP/GDP and other site procedures assigned

• Providing various reports from SAP to support the Quality Function at GWWO

• Providing timely and pro-active SAP support in various SAP GWWO projects

• Delivery of training in SAP for new employees, if required

• Participation in the completion of Deviation, CAPA and Change Control processes, as required

• Other duties as instructed by the SAP Quality Supervisor/ Quality Systems and Compliance Manager/ Technical Director

. Person Specification

Qualifications

Minimum of B.Sc Degree or equivalent third level education and at least 5 years’ experience in quality within the pharmaceutical/medical devices industry.

Knowledge and Skills

• A strong background in Quality Control and Quality Assurance

• Previous experience in working the pharmaceutical GMP or medical devices environment

• Experience in SAP ECC as a Quality super user

• Good problem solving and continuous improvement skills

• Ability to work accurately under pressure

• Ability to handle multiple projects and deadlines

• Good communication skills and the ability to collaborate at a variety of levels within and outside the organisation

• Ability to work on own initiative

• Proven success working well in a team environment with flexibility to react to changing business needs, as well as demonstrated problem solving and project management ability.

• Extensive knowledge in a broad range of pharmaceutical activities and Quality Systems.

• Ability to work in a dynamic environment and to constantly redefine the scope of responsibilities in alignment with compliance and business needs

• Ability to multi-task and prioritise work

• Strong organisational ability

Our Benefits Include:

• Highly competitive salary

• Group pension scheme - Contribution rates are (1.5% / 3%/ 5%/ 7%) and company will match

• Private Medical Insurance for the employee

• Ongoing opportunities for career development in a rapidly expanding work environment

• Succession planning and internal promotions

• Education allowance

• Wellness activities - Social activities eg. Padel, Summer Events

We understand that self-doubt can hold talented individuals back from applying for opportunities. We encourage everyone who meets the qualifications to apply – we're excited to hear from you

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Learn more about Grifols (http://www.grifols.com/es/web/international/home)

Req ID: 527589

Type: Regular Full-Time

Job Category: