Grifols Veterans Jobs

ces they need to deliver expert medical care. </p><img src="http://www.grifols.com/documents/239901/1137346/SuccesFactors_1020x93_jobposting_line_test.png/ec7da48f-8161-41cb-b53a-7a36f6a376a6" width="100%"><p><strong>Position Summary </strong></p><p>To complete an
able.MiTabla { max-width: 1020px;!important </p><img align="top/" alt="" src="http://www.grifols.com/documents/239901/3495811/SuccesFactors_1020x93_jobposting_IRL.jpg/f00e8666-0e9f-436f-a392-3ec697c8ac17"><p style="text-align:justify">For more than 75 years, Grifols has worked to
ientated </p><p><img src="http://www.grifols.com/documents/239901/1137346/SuccesFactors_1020x93_jobposting_line_test.png/ec7da48f-8161-41cb-b53a-7a36f6a376a6" width="100%"></p><p></p><p></p><p><a href="http://www.grifols.com/es/web/international/home" target="_blank">Learn more about Grifols </a></p><p></p><br><strong>Req ID: </strong> 121707 <br><strong>

Job Information

Grifols Shared Services North America, Inc QA Packaging Technician in dublin, Ireland

For more than 75 years, Grifols has worked to improve the health and well-being of people around the world. We are a global healthcare company that produces essential plasma-derived medicines for patients and provides hospitals and healthcare professionals with the tools, information and services they need to deliver expert medical care.

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).

Key Responsibilities

Communication:

Daily briefing on Quality batch review/approval

Provide quality performance information as required

Ensure regular Quality interaction with other Departments

Quality Release Activities:

Material release – testing of raw materials and ID testing finished product

Sampling of raw materials/packaging

Quality batch documentation review and control

Quality in-process control including vial defect inspection

Customer complaint investigation

Annual product quality reviews

Support the process change control system

Support the quality audit/inspection programmes

Process/product/system improvement projects

Provide Quality input to process/product investigations (including planned / unplanned deviation)

Provide information to Regulatory Affairs as required

Training of new Quality personnel where appropriate

Review of Batch Records and SOPs

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.

Keep abreast of the latest developments from regulatory authorities in relation to Quality Compliance activities.

Key Responsibilities

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

Learn more about Grifols

Req ID: 121707

Type: Regular Full-Time

Job Category: Quality

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