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Validation Engineer

  1. Ireland, Cork
Cork
  1. Contract
Competitive
  1. Life Sciences
33823
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Validation Engineer - Pharmaceutical - Cork, Irleand - 8-Month Contract 

Do you want to be involved with exciting Pharmaceutical projects?

When it comes to the development and production of veterinary vaccines, our pharmaceutical client has the largest centre in the industry worldwide and is a Centre of Excellence; employing more than 1000 people. They are looking to add to their team and require a Validation Engineer.

This a fantastic opportunity to be involved with the critical investment projects both on-site and remotely.


What skills you will need:

In order to excel in this role, you will need to have:
  • Extensive experience as a validation specialist in a pharmaceutical or a highly regulated environment and a B.Sc. Degree or other qualification in Chemical Engineering, Biochemistry, Microbiology, Chemistry or a related field.
  • Experience in at least three of the following areas: C&Q validation, Cleaning Validation, Equipment validation, Process operations or manufacturing, Process Engineering.
  • A working knowledge of the GxP systems associated with this role would be advantageous. These include, but are not limited to:  GLIMS and eVAL, electronic batch records.

Requirements: 
  • Execute cycle development, cleaning validation and PQ of equipment.
  • Writing and adhering to validation strategies, coordinating with outside vendors, writing protocols independently, sample submission, analysing test results, and preparing technical reports.
  • Execute run the business activities e.g. equipment periodic reviews, cleaning periodic review, CAPAs and deviations, change control, risk assessments.
  • Provide support during commissioning phase by reviewing and approving documents. Ensure documentation complies with standards.
  • Part-take in cross-functional problem-solving teams for troubleshooting and investigations within Vaccines IPT
  • Technical report writing, statistical analysis of data
  • Adherence to the latest regulatory guidelines.
  • Represent the IPT on cross-functional project teams.
  • Provide technical input and support and present as an SME on relevant topics during regulatory inspections.
  • Adherence to highest standards for Compliance (Quality and Safety)

If this role is of interest to you, please apply now! 

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