We are currently looking for a QC Data Reviewer to join a leading Pharmaceutical company based in Ireland. As the QC Data Reviewer you will be responsible for monitoring the quality of laboratory data and reports while also being a point of contact for results internally and to external sites. KEY DUTIES AND RESPONSIBILITIES: Your duties as the QC Data Reviewer will be varied however the key duties and responsibilities are as follows: 1. Responsible for defining, managing and maintaining a documentation control system for QC cGMP Documents. 2. Responsible for reviewing QC testing data ensuring compliance to procedure, specifications, data integrity and cGMP standards. 3. Support to identify OOT and OOS results and escalate as appropriate 4. Responsible for maintaining Good Documentation Practices (GDP) including laboratory documentation and analytical reports ROLE REQUIREMENTS: To be successful in your application to this exciting opportunity as the QC Data Reviewer we are looking to identify the following on your profile and past history: 1. QC Data Reviewer experience within a GMP environment. 2. Good Documentation Practices (GDP) experience. 3. Ability to demonstarte the ability to follow an efficient and consistent data review process. Key Words: QC / Data / Reviewer / Analyst / GMP

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