Company Description
Impact Engineering Ltd is a trusted automation partner based in Dublin, focusing on business transformation, digitalisation, automation projects, and targeted automation training. We offer a range of services including consultancy, system upgrades, process optimization, and automation front line support. Our mission is to deliver innovative, cost-competitive, and compliant automation solutions to add value to businesses through digitalization.
Role Description
This is a site based contract role for a CQV Engineer at our customer site, based in Northern Ireland. This position is a key element of a project team that will be based on site. In this role you will be expected to:
* Take part in the planning, execution, and oversight of CQV activities to ensure that automated systems meet predefined requirements and operate within validated parameters.
* Create and maintain validation documentation, including protocols, test scripts, and validation reports.
* Ensure that all automation systems comply with industry standards, GxP guidelines, and regulatory mandates.
* Maintain accurate and organized documentation for all validation activities, including equipment and software specifications, validation protocols, and records.
* Collaborate with our client to ensure the proper documentation of automated system configurations.
Qualifications & Experience
* Bachelor’s degree in engineering or similar.
* 5+ years working experience as CQV Engineer on Pharmaceutical or Biopharmaceutical projects or comparable experience
* Experience with DeltaV is preferred
* On site project experience is essential.
* Ability to work on site every day
* Ability to interact and communicate with other engineering and business disciplines.