Due to a new project coming on board at one of our customer sites, we are currently looking for a number of validation engineers to join our team. Reporting to the Stericycle GxP Senior Management, this is a tremendous opportunity for any validation engineer.
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...
Due to a number of new projects coming on board, Stericycle GxP Solutions have a requirement for a Software Engineer with a minimum of 2 years industry experience to join our team. Reporting to Stericycle GxP Senior Management & the customers' on site Equipment Manager, the Software Engineer must be legally permitted to work in EU. The successful candidate will assist R&D and Operations on New Product Development Programs and Sustaining Prog...
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...
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.