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Process Engineer, Minimum 10 years' experience in Biologics Process Engineer Work with process automation, equipment engineers and all technical groups - Set up and review processes for aseptic and sterile injectable technologies and equipment. Suggest and select process equipment for new fit outs or upgrades, including supplier selection
Currently, we are recruiting an Experienced Project / Process Engineer. Veolia Water Technologies is the largest provider of High Purity Process Water Systems in Ireland operating primarily in the Pharma; Biotech; Healthcare; Research; Food & Beverage; and Micro-Electronics Sectors.
A thriving start-up company in Dublin are looking for a Process Engineer to join their team. If so, you could be the Process Engineer that we've been looking for. As a Process Engineer, you'll offer technical expertise to clients, in order to ensure that they meet their market forecasts.
Our client, an API centre of excellence of an international company, is seeking to recruit a Snr Process Engineer to manage various activities on site. • Take responsibility for the oversight of commercial Products from a process engineering perspective. Design how new manufacturing processes will be implemented in commercial manufacturing plants.
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To coordinate manufacturing activities for the manufacture of R&D scale up, clinical batches within the pilot plant/production facilities in support of any submission processes. To ensure the maintenance of processes and procedures and general cGMP status of the Pilot Plant at all times in line with requirements of IMP License.
You will be involved in delivering on key process, quality, safety, maintenance and production goals in a highly automated manufacturing environment. o Process improvement through identification of problem areas/opportunities for improvement and engineering the necessary changes, following up with production, tool room and outside resources as appropriate.
The senior process engineer will thrive in fast pace and challenging environment and will coordinate manufacturing activities for the manufacture of R&D scale up, clinical batches within the pilot plant/production facilities in support of any submission processes.
Ensure operators, engineers and supervisors are trained on new technology, new products and new processes/operations and encourage feedback so that equipment performance may be optimised. Study, evaluate and document existing processes and highlight areas on systems where errors or potential errors may occur.
Validation Engineer required for a Pharmaceutical Client in the Midlands. Validation Engineer - Pharmaceuticals DPS is a leading Project Management and Engineering Company serving industry around the world for over 40 years.
The role primarily focuses on leading/supporting process investigations at the request of the OpU. The role also focuses on routine process technical support and troubleshooting for the Suite. Currently the Suite is manufacturing demonstration batches and will go into Process Validation in Q1 2018.
Senior Process Engineer required or our client a leading pharma company in Dublin. You will work as a Senior Process Development Engineer for our client, a leading pharma company in Dublin.
The Technology Support Engineer will provide technical support to our enterprise partners to ensure their Easytrip systems and operations run in an effective and efficient manner. Working directly with installation engineers to coordinate the planning, installation and rollout of new sites.
You will join a team of engineers who drive innovation, deliver industry leading solutions and thrive in using and applying new technologies for Data/Analytics, Robotic Automation, AI and Machine Learning. The Custody and Fund Services (CFS) Technology group designs, builds and operates applications that support the world’s leading asset management firms.
I am are currently seeking a Project Mechanical Engineer to join the Engineering team based in North County Dublin. Responsibilities - Design of mechanical equipment to specific customer requirements - Ensuring that all engineering documentation created as part of tasks meet the requirements of internal procedures & strict timelines.
In addition to this you will be involved in upgrading, patching, executing and monitoring the processes that keep the Workday Service up and running in all environments: production, sandbox, implementation, sales, training, partners etc. You'll do everything from creating scripts, applying patches and updates to all our systems ...
My Client currently have a requirement for an Electrical commissioning & qualification (C&Q) Engineer based in Louth. The Electrical commissioning & qualification engineer will be primarily responsible for providing input into all aspects of C&Q i.e. from design through to commissioning and qualification completion.
The client’s overall business objective is to employ Lean management systems / operating systems / mind-sets and behavioural tools & techniques to engage and energise associates to install a continuous focus on the end-to-end process from a customer perspective.
The successful candidate will join the Global Device Development team as a Device Development Assurance Engineer/ Scientist working in collaboration with Mylan QA function. For Us, It's a Mission - At Mylan, we mean it when we say we work every day to provide access to high quality medicines to the world's 7 billion people.
the Global Device Development team as a Device Development Assurance Engineer/ Scientist. 12 month Fixed Term Contract - For Us, It’s A Mission - is a global pharmaceutical company committed to setting new standards in - healthcare. Working together around the world to provide 7 billion people - access to high quality medicine, we innovate to satisfy unmet needs; make
The Lead Commissioning and Qualification Engineer at Commissioning Agents, Inc. develops the documentation to support C&Q, manages a portfolio of projects from a C&Q perspective and protocol execution. The Lead Commissioning and Qualification Engineer at Commissioning Agents, Inc. develops the documentation to support C&Q.
CAI is looking for Computer System Validation (CSV) Engineers at least 4 years of experience working in a GMP environment. The Computer Software Validation (CSV) Engineer at Commissioning Agents, Inc. will author and execute protocols and test scripts.
Validation Engineer required for a large Medical Device client based in Dublin. Assist other Engineers and external vendors regarding equipment User Requirement Specifications (URS’s) and design activities (DQ). Must have experience in a high volume regulated manufacturing environment.