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.
Overview
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.
Responsibilities
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
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.
Seniority level
Mid-Senior level
Employment type
Full-time
Job function
Engineering, Information Technology, and Manufacturing
Industries
Pharmaceutical Manufacturing
Automation Machinery Manufacturing
Biotechnology Research
#J-*****-Ljbffr