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QA Validation Specialist

  1. West
  1. Contract
  1. Commisions, Qualification and Validation
Date Posted26 Jun 2020

This vacancy has now expired

QA Validation Specialist, Global Pharmaceutical Company, Ireland

Ireland is a hive of activity for the Life Sciences Sector at present with global players setting up new and expanding existing manufacturing facilities all over the Country.

An exciting opportunity has arisen to work via Quanta on the client’s side for a global Pharmaceutical organisation on a major expansion project based in the picturesque Munster region of Ireland. 


This position implements policies and procedures to review site Change controls, Technical Evaluations and Test plans for equipment, systems, and processes in accordance with regulatory requirements and company manufacturing standards.

Essential Duties and Responsibilities include, but are not limited to, the following:
  • Strong Quality background and familiar with Site change controls in general.
  • Reviews Change Control test plans generated by the Engineering/Automation/Manufacturing teams against standard operating procedures and policies.
  • Assists in projects by helping to develop appropriate plans, schedules and other project deliverables as required. 
  • Collaborates with functional departments to resolve issues.
  • Excellent communication skills is a must.
Education and Experience:
  • Requires a BS/BA in Engineering, Chemistry, or Life Sciences with a minimum of 3+ years of related experience within the field; may consider substituting relevant experience for education.

If this role is of interest, please apply now.  

The candidate must have the rights to work in the location stated in the job advert.

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