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Validation Engineer

  1. Dublin
  1. Contract
Competitive
23488/NK
  1. Life Sciences
Date Posted08 Oct 2019
Ireland is a hive of activity for the Life Sciences Sector at present with global players setting up new / 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 one of their existing manufacturing facilities in County Dublin. 

Located within a short drive of Dublin airport, the manufacturing site is workable for those wishing to commute to/from Ireland for a contract position. You will be required on site for 5 days per week Monday – Friday working 39 hours.

The Role:

We are looking for an Equipment Validation Engineer to join this Pharmaceutical company for 6 months. The overall objective of this role is to partake, validate and support a portfolio of project activities on site including new process installations, process modifications and process improvements relating to manufacturing, facility & packaging operations unit.

Day to day duties will include:
  • Supporting capital projects team for on-site based projects for Manufacturing, Facilities and Packaging operations.
  • Perform activities in support of the validation program such as risk assessments and review and assessment of development data in line with recognised standards.
  • Responsible for development, approvals control, execution and closure of the Validation Project plan for all tests.
  • Responsible for retrospective reviews and update of existing validation system or documents.
  • Ensure completion of Risk Assessments
  • Ensures that all deviations to protocols and/or deviations to acceptance criteria are adequately controlled, documented and addressed by the Validation / Engineering Team.
  • Provides guidance in closing out noncompliance and deviations in relation to Validations.
  • Provides assistance and ensures the preparation of validation protocols, process design specifications and associated documentation for equipment and systems.
  • Participates in project teams and assists in determining project schedules and the relevance of appropriate levels of validation
The ideal candidate will have the following experience:
  • Validation Engineer experience within a Pharmaceutical Manufacturing / Packaging facility.
  • Ability and proven track record in working and managing multiple departmental teams for operational and capital projects.
  • Strong documentation skills
  • May require some travel within Europe, depending on project but will be minimal.
Get in touch today for immediate consideration!

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