Job Archives
Responsibilities This candidate will be required to work closely with the site AIT teams responsible for the full Automation and IT scope and with vendors / partners with responsibility for deliver...
Responsible for providing process, technical, and validation support operations including ongoing support of manufacturing processes and support for new product introduction. Accountable for analytica...
Generate/ update, execute, review and approve Computer System Validation (CSV) documentation deliverables as part of a multi-disciplinary team of site representatives responsible Process Automation Re...
The site Labs CSV Engineer will be responsible for delivery of Automation and IT scope on one or more lab projects in the portfolio of capital projects. This candidate will be required to work closely...
Process Validation Technology Transfer Specialist The Process Validation Technology Transfer Specialist will be responsible for developing Validation and Technical Standards and Guidelines f...
Lab CSV Engineer This is a contract role in a well-known, multinational Pharmaceutical Manufacturing site based in Dublin. The Lab CSV Engineer will work with internal and external teams to ens...
Qualified Person The Qualified Person is responsible to ensure that licensed Finished Product to include Drug Substance, Drug Product is certified and released to market by a Qualified Person named...
Technical Specialist The Technical Specialist, will be responsible for providing scientific and technical support of drug substance manufacturing processes. The successful candidate will be respons...
Project Controller Our leading international pharmaceutical client is looking for an experience Project Controller to join their team in Cork. The Project Controller will review, coordinate, ...
The successful candidate will join the QA IT team on a site expansion project to provide independent compliance oversight and support for the implementation of new laboratory systems. The QA IT spec...
Responsibilities Ensure the appropriate quality documents as needed for the Life-Science industry, such as Quality Assurance (QAPs) test plans, Quality assurance summary reports (QASR) are in place...
Responsibilities The OEM Area lead will drive the development and provision of all associated OEM Systems /Equipment. Manage the Design and development of OEM hardware and Software Components, and ...
Reporting to the site AIT OEM Lead, specifically responsible for OEM Systems. This candidate will be required to work closely with the site AIT teams responsible for the full Automation and IT scope a...
Reporting to the site DeltaV Lead, supporting delivery of DeltaV scope on the project(s). This candidate will be required to work closely with the site teams responsible for the full Automation and IT...
You will be a member of the Automation & PI/MES team reporting to the Site Manufacturing Systems Lead, specifically responsible for both project support and fault-finding / support of production u...
