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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 : To complete and support activities within the Quality Department relating to GMP Compliance and raw material/product release. To provide Quality support for the manufacturing operations in Grifols Worldwide Operations Ltd (GWWO). 

Communication

Daily briefing on Quality batch review/approval Provide quality performance information as required Ensure regular Quality interaction with other Departments Attend tier meetings to provide datails of any quality issues

Activities 

Supervision of quality technician team Material release   Supervision of sampling, ensure sample reviews and distruction is complete ontime  Supervise all quality in-process control activities including vial defect inspection Quality batch documentation review and control when required Material status assignment Support customer complaint and deviation investigations Support product recall activities Support the process change control system Support the quality audit/inspection programmes Process/product/system improvement projects Drive and oversee process/product/OOS investigations (including planned / unplanned deviation) Facilitate Inspections by third parties, e.g. HPRA, FDA, customers, etc.

To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.

 Excellent communication skills Competence in Microsoft packages specifically word, excel and PowerPoint, SAP and other systems such as DCM Good organizational skills  Results orientated Minimum of B.Sc Degree or equivalent third level education and at least 2 years’ experience in a quality or production function within the pharmaceutical industry Excellent technical writing and analytical skills Desirable - Previous experience in audits participation

Our Benefits Includes: 

Highly competitive salary Group pension scheme - Contribution rates are 5% employer and 5% employee 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. Golf, 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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Location: Dublin:Grange Castle