Our customer, a leading provider of new and innovative medical device products based in Galway require an Equipment Validation Engineer. Reporting to the Stericycle GxP Project Supervisor and working as part of the on-site customer engineering team, the Equipment Validation Engineer will be responsible for preparation of the equipment documentation.
Due to an increase in production and activity at one of our customer sites, we are now looking for an extra Validation Engineer resource to join our team. Reporting to Stericycle GxP Senior Management and the on site Engineering Manager, you will be responsible for completion of validation activities surrounding equipment, processes and systems.
The successful candidate will assist R&D and Operations on New Product Development Programs and Sustaining Programs by participating on the Design, Build, Commissioning and Qualification of New Equipment as well as Equipment Upgrades. The Role is primarily based in Connacht although traveling abroad may be required from time to time and for short periods. Working times are Monday to Friday; however Weekend work may be required. Although not n...
The CSV Engineer, reporting to the Quality Manager, will be involved in ensuring that the installation and qualification of Quality Management System (QMS) computer software onsite is complete in accordance with cGMPs, GAMP, 21 CFR Part 11 and other applicable regulations. This position will assist in liasing with the vendor, preparing/reviewing documentation and will engage in activities to support commissioning, validation, and qualification...
CSV Engineer, Software Validation Engineer
Stericycle GxP Solutions have openings for a number of Automation Engineers to join our established team & work with us on a customer site - one of the largest medical device manufacturers in the world. Based in a manufacturing facility Limerick, the Engineer will be report to Stericycle GxP Senior Management and the customers' in-house Automation manager.
Validation Engineer required for new project at an existing customer site based in Galway, Ireland. Reporting to the Stericycle GxP Project Lead, the Validation Engineer will provide a wide range of validation activities to a new manufacturing line at the facility. Medical Device Industry experience is essential for this project.