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Quality Data Specialist

  1. Ireland, Dublin
County Mayo
  1. Contract
Competitive
  1. Data Centres
35771

This vacancy has now expired

Quality SAP Master Data Specialist - County Mayo - 9-Month Contract 

Located on the picturesque west coast of Ireland, our Global pharmaceutical client is looking for a Quality Data Specialist to join their state-of-the-art pharmaceutical facility. They have invested $55 billion in research to discover and develop new medicines in the pursuit of scientific breakthroughs and changing people’s lives. They have 50,000 employees around the world and are continuing to grow.


Responsibilities:
  • Be an active member of the Quality Master Team to support the Company's succession planning.
  • Sustain the culture of Quality across the Quality Master Data team.
  • Foster a strong working relationship with relevant global functions as it relates to SAP master data and the performance of the company quality and compliance.
  • Foster a strong working relationship with other master data stakeholders such as supply chain, procurement and operations.
  • Participate in Master Data projects & coordinate with stakeholders to ensure master data milestones are met
  • Manage & analyze workflow data requests for compliance, accuracy and completeness
  • Follow robust procedures for the creation and approval of SAP Quality Views, Inspection plans, Quality Status records and Quality Information records.
  • Create (where necessary) and approve all DSP master data requests relating to SAP Quality master data.
  • Maintain SAP inspection plans for all incoming and manufactured materials

Qualifications:
  • Degree or 3rd level qualification (Business, Science, Engineering)
  • Advanced degree, diploma or certification in Data or Supply Chain Management preferred
  • Extensive SAP Master Data experience in the Manufacturing environment, preferably in the pharmaceutical industry
  • Experience in setup of master data business processes
  • SAP Master data experience should include excellent understanding of Material Master, purchasing, BOM, Routing, Quality etc.
  • Possess  analytical skills in data management, interpretation, and reporting
  • In-depth and current knowledge of all relevant GxP and Quality System requirements (US, EU) for pharmaceutical and biotech, manufacturing and related activities.
  • Excellent communication & interpersonal skills that enable effective working relationships with internal/external stakeholders.

 If this role is of interest, please apply now!

 #LI-JS4
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