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Principal Consultant – Quality/Scientific

I am looking for a Quality Associate to join a Pharmaceutical Manufacturing organisation based in Speke, UK who can support third party quality operations at EEM EMEA and ensure that third party products are produced and released according to company requirements and to operate and maintain quality systems which monitor the compliance of third party manufacturers and products.

Functions, Duties, Tasks:

• To perform QA oversight on assigned external suppliers and third parties manufacturing product and ensuring, that the delivered products comply with quality standards and legal requirements.
• To monitor third party KPI’s to proactively detect and notify to QA management any compliance issue on supplier level that would risk supply of products.
• To review and assess external customer complaints in the global complaint system, including Root Cause Investigation correctness, product impact assessment, trend/recurrence evaluation, and proposed CAPA assessment, within the due time periods.
• To review and assess Third-Party deviation reports for correctness/completeness, including Root Cause Investigation, assessment of product impact, trending/recurrence evaluation, and suggested CAPA.
• To review batch release documentation provided by third parties to support or act as Authorized Person for release of products for shipment including material status change in SAP.

Preferences:

• Experience in customer complaint handling;
• Experience in the negotiation QA contracts;
• Experience in QA systems that support Third Party management;
• Working experience within a global organization.

12 Month initial fixed term contract

3 days in Speke, UK 2 days work from home

Payrate between £20/25 per hour

If you are interested, please send your updated CV to jamie.keith@cpl.com

Seniority level

• Seniority level

  Associate

Employment type

• Employment type

  Contract

Job function

• Job function

  Quality Assurance

• Industries

  Pharmaceutical Manufacturing

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