SimoTech provides manufacturing automation and IT systems engineering, project management and validation services. We partner with life sciences companies to design, build, operate and optimise critical process automation systems that deliver fast track project delivery, operational efficiency, improve manufacturing agility and achieve regulatory compliance.
Why SimoTechWhat is it like to work at SimoTech? With a strong collaborative teamwork culture based on respect, trust and excellence, we play a critical partnering role to our clients' life-changing supply of products to patients. In return, there is excellent salary, career progression, educational support and much more.
SimoTech has a new opportunity for a highly skilled Automation Engineer with a minimum of 5+ years' experience to join our team supporting our client, a leading Life Science company in Dublin.
The Automation Engineer will be responsible for the design, development, and maintenance of automated systems in compliance with industry regulations. The ideal candidate will have experience in process and building automation, PLC/SCADA, PCS and BMS systems, and working within GxP environments.
Key ResponsibilitiesDesign, program, and implement automation solutions for manufacturing processes and critical systems, ensuring they meet operational and regulatory requirements.Collaborate with cross-functional teams to develop control strategies and integrate new automation technologies into existing systems.Participate in the installation, commissioning, and qualification (IQ/OQ/PQ) of automated systems and equipment.Ensure all automation systems meet the necessary GMP, GxP, and FDA regulatory standards.Prepare and review validation documentation, including test protocols, reports, and design specifications.Provide technical support for automated systems, diagnosing and resolving any hardware, software, or process issues.Ensure that all changes are documented according to change control processes and regulatory guidelines.Adhere to data integrity principles and ensure automation systems are compliant with 21 CFR Part 11.Work closely with process engineers, IT, quality, and validation teams to ensure seamless integration and operation of automation systems.Liaise with vendors and third-party contractors during the design, installation, and support of automation systems.QualificationsMinimum of 5+ years of experience in automation engineering within the life sciences industry (pharmaceuticals, biotechnology, or medical devices).Minimum 3 days per week required on Site.The preferred candidate will have experience working with Siemens Desigo BMS.Strong understanding of GMP, GxP, and FDA guidelines and their impact on automated systems.Proficiency in PLC programming (Siemens, Allen Bradley) and SCADA systems (e.g. iFix, Intouch).Experience with PCS systems (PCS7) and system integration.Strong knowledge of networking protocols (e.g., Ethernet/IP, Modbus, OPC).Strong problem-solving skills with the ability to troubleshoot and resolve complex automation issues.What SimoTech Can OfferRole provides a high degree of autonomy to allow the successful candidate to reach their full potential.Develop new skills and enhance technical ability by working with innovative technologies in a multi-disciplined environment.Opportunity to work with large corporate clients on exciting capital projects.By submitting my data (CV), I consent to SimoTech collecting and storing my personal data, as outlined in the SimoTech Privacy Statement which I have read.
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