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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.

A QA Packaging Technician is required to complete and support activities within the Quality Department relating to GMP Compliance and product release. To provide Quality support for the packaging operations in Grifols Worldwide Operations Ltd (GWWO)

This is a 3 cycle shift pattern, It is a 12 hour shift work. A combination of Day and Night

What your responsibilities will be:

Communication:

• Daily briefing on Quality batch review/approval

• Provide quality performance information as required

• Ensure regular Quality interaction with other Departments

Quality Release Activities:

• Quality batch documentation review and control

• Quality in-process control including vial defect inspection.

• Quality visual inspection of Media fill and filled product bags

• Participation in internal and spot check audits

• Support the quality audit/inspection programmes

• Process/product/system improvement projects

• Provide Quality input to process/product investigations

• Training of new Quality personnel where appropriate

• Review of Batch Records

• GMP implementation and site-wide Quality Awareness.

• Follow up corrective actions identified through the Deviation system.

• Liaise with other Department representatives to promote improvements in GMP and Quality standards.

All listed tasks and responsibilities are deemed as essential functions to this position; however, business conditions may require reasonable accommodations for additional task and responsibilities.

Who you are

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

• 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 communication skills

• Competence in Microsoft packages specifically word, excel and PowerPoint

• Good organizational skills

• Flexibility

• Results orientated

• Excellent technical writing and analytical skills

• Desirable - Previous experience in audits participation

Our Benefits Include:

• 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. Padel, Summer Events

If you’re interested in the rol eand you have what it takes, then don’t hesitate to apply.

We look forward to receiving your application.

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

Req ID: 518903

Type: Regular Full-Time

Job Category: