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SL Controls Ltd
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  • Senior Validation Engineer  

    - Kilkenny

    The Role: Senior Validation Engineer Kilkenny Onsite Contractor or Permanent opportunity Role Brief: The successful candidate will focus on the validation activities for a range of equipment & process solutions within a regulated Pharma environment. You will both have responsibility for a number of activities and pieces of equipment while also supporting the wider Validation function and ensuring Validation activities are closed out in line with the Validation Master Plans. Skills Brief: Managing & coordinating the preparation, review & approval of Validation Master Plans Generate, execute and review validation protocols and associated reports for related equipment and processes. Managing & coordinating all validation strategies & deliverables Managing & coordinating the preparation, review & issuing of validation protocols & reports Managing & coordinating validation documentation (risk assessments, traceability matrices) Managing & coordinating the review & approval of specifications associated with Equipment & Processes. Managing & coordinating routine Internal Quality Audits of the facility to ensure compliance & be proactive in resolving issues that may arise. Provide technical direction & hands-on assistance for testing projects Person Brief: Candidates must have a Bachelor’s degree in Computer Science, Electrical Engineering, Systems Engineering, Technology or a related discipline with over 3 years’ experience of Validation Engineering experience. You should ideally have at least 1 years of experience of Validation activities for equipment found in Pharmaceutical or other GMP regulated environments. The ideal candidate will have excellent collaboration and communication skills, strong attention to detail and an excellent understanding of validation concepts and documentation. He/she should also have proven ability to solve complex technical & equipment qualification challenges using a rational scientific approach. The candidate should be based in Kilkenny or within a reasonable commute as this will be a fully onsite position. Opportunity Brief: This is an excellent opportunity to work with clients who are global leaders in their field, helping to develop and improve upon industry leading technology solutions. SL Controls offers a supportive environment committed to employee development and wellness, along with a competitive and rounded compensation package, which rewards high performers. Company Brief: SL Controls are experts in the area of Equipment System Integration and System Support. We specialise in assisting our customers, including many of the world’s top multinational companies in the medical device and pharmaceutical sectors, achieve their Six Sigma and OEE targets. Over the past 20 years we have grown our business from a Sligo based enterprise into an international business with additional offices in Galway, Limerick, Leinster and Florida USA. We pride ourselves on our expertise in industrial IT integration and regulatory compliance in support of global end users, OEM’s and Technology providers. Find out more about working at SL Controls , our Sustainable Development Goals , and our Diversity, Equity, and Inclusion policy . #J-18808-Ljbffr

  • Project Manager  

    - Dublin Pike

    The Role: Project Manager Dublin Hybrid Role - 2 to 3 days per week typically will be required onsite, however you must be available to be onsite as per project requirements and this may require more than 2 to 3 days per week at times Contractor Opportunity Role Brief: The successful candidate will manage a project for an NNIT Ireland client that will focus on the decommissioning of a pharma packaging system. This project is of a large scale involving multiples lines and it will involve both line decommissioning and transfer activities. Key duties: Identification of all key stakeholders for project success. Establishment of core project governance to maintain quality of project delivery. Manage project documentation and artifacts. Manage project life cycle documentation, like Risk Management, Risk Log, Business Impact Assessment, Project Schedule, Project Task List, Timeline, Communication Documentations etc. Procurement of hardware, services, and resources, as needed. Work with application/system owners and architects for discovery and gap analysis. Develop test plans with stakeholders. Manage the upgrades and adjustments to architecture and ancillary platforms. Manage training and testing. Manage cutovers planning and go-lives. Skills Brief: Project Management experience in managing end to end projects involving a range of automation systems and other integrated systems. Proven working experience in managing cross functional teams. Good understanding of industrial automation technologies such as PLC systems, SCADA, OPC, Continuous/Batch Historians and MES systems including network topology concepts. Scrum Master certification is a plus. Project Management professional fluent with waterfall, critical path management, agile frameworks, and tools. Experience of drafts validation document lifecycle, including installation/operational qualification and design specification creation and execution across multiple successful projects, of varying scope. A proven ability to coordinate work with vendors and contractors, during project conception and implementation stages. Experience of implementing and delivering large projects in complex GMP (Pharma, Life Sciences, Medical Devices) manufacturing environments is essential. Candidates without 2 or more years experience in this sector and exposure to delivering at least 2 large scale projects will not be considered. Complex Project Management experience in fast-paced environment. Person Brief: Candidates must have a bachelor’s or master's degree in Mechatronics/Automation/Mechanical/Electrical Engineering or Computer Science or a related technical discipline. 5 years’ experience in supporting and managing industrial automation and systems integration projects with some of this experience gained in a GMP (Pharma, Life Sciences, Medical Devices) environment. The ideal candidate will have excellent communication and teamwork skills that inspire others and have experience in leading cross-functional teams on complex technical challenges. The ideal candidate should also have an agile mindset and the ability to adapt to and manage change. Vendor Management experience is essential for the role. A PMP / Prince / PgmP Certification is advantageous for the role. Knowledge of Agile Frameworks is a definite requirement. Based within a commutable distance of the Dublin based manufacturing site or able to relocate within 1 to 2 months maximum as you will be required to be onsite a number of days each week. Opportunity Brief: This is an excellent opportunity to work with clients who are global leaders in their field, helping to develop and improve upon industry leading technology solutions. NNIT Ireland offers a supportive environment committed to employee development and wellness, along with a competitive and rounded compensation package, which rewards high performers. Company Brief: NNIT Ireland are experts in the area of Equipment System Integration and System Support. We specialise in assisting our customers, including many of the world’s top multinational companies in the medical device and pharmaceutical sectors, achieve their Six Sigma and OEE targets. Over the past 20 years we have grown our business from a Sligo based enterprise into an international business with additional offices in Galway, Limerick, Leinster and Florida USA. We pride ourselves on our expertise in industrial IT integration and regulatory compliance in support of global end users, OEM’s and Technology providers. #J-18808-Ljbffr

  • Software Engineer - MES  

    - Monaghan

    The Role: Software Engineer - MES Donegal Onsite Role Permanent or Contractor role Role Brief: This role will be responsible for the maintenance of the POMSnet Manufacturing Execution System (MES) environment. You will maintain recipes and worksheets for the manufacturing site using the POMSnet system. Core Responsibilities: Design and development of MES systems. Assisting with MES, Database and system upgrade related tasks. Work as part of a team in designing and developing electronic batch records / workflows within the MES solution. Support, troubleshoot and resolve issues within the system. Identify and drive continuous improvement opportunities within MES solution. Skills Brief: A Bachelor’s degree in computer science or an IT related discipline is preferred or a highly related qualification in mechatronics or manufacturing engineering will also be considered. Experience in an IT/Software focused role in a GMP (Pharma, Life Sciences, Medical Devices, Biotech) manufacturing environment is essential and only candidates with some experience in this area will be considered. Oracle Manufacturing systems (OMD) experience would be required for this role. Experience in C# coding and SQL database knowledge. Strong learning agility. Ability to proactively identify technical IT issues and either resolve or escalate to the appropriate level for resolution. Experience of software validation within the medical devices industry would be highly advantageous. Person Brief: 1 year plus experience working in an IT Software / MES Software environment with direct manufacturing industry exposure is essential. Strong analytical, troubleshooting, written & verbal communication skills are essential. The role is based onsite in Donegal so you must be living in the area or able to relocate in a short time frame and be able to be onsite daily. Opportunity Brief: This is an excellent opportunity to work with clients who are global leaders in their field, helping to develop and improve upon industry leading technology solutions. NNIT Ireland offers a supportive environment committed to employee development and wellness, along with a competitive and rounded compensation package, which rewards high performers. Company Brief: NNIT Ireland are experts in the area of Equipment System Integration and System Support. We specialise in assisting our customers, including many of the world’s top multinational companies in the medical device and pharmaceutical sectors, achieve their Six Sigma and OEE targets. Over the past 20 years we have grown our business from a Sligo based enterprise into an international business with additional offices in Galway, Limerick, Leinster and Florida USA. We pride ourselves on our expertise in industrial IT integration and regulatory compliance in support of global end users, OEM’s and Technology providers. #J-18808-Ljbffr

  • IT Business Analyst  

    - Monaghan

    The Role: IT Business Analyst Donegal Onsite Role Permanent or Contractor role Role Brief: The IT Business Analyst will operate as the liaison between the IT and Business functions. Your role will be to formulate business requirements to solve a range of business problems. You will work with a range of stakeholders and consult with a range of personnel to develop and understand business cases and requirements. You will drive department-level initiatives whilst also aiding Program and Project managers on larger project phases as required. Core Responsibilities: Responsible for compliance with applicable Corporate and Divisional Policies and procedures. Performs work using existing standards, methodologies, and processes and understands other systems/business processes relationship to each other. Assist in preparing, developing, and conducting clients and systems training. Completes project tasks within time and budget constraints. Identifies and implements process improvements. Maintains productive relationships with peers and management in IT and the business function. Skills Brief: Essential: IT experience working in large or midsized multinational organization. Good understanding of IT system applications, including the infrastructure. Good organizational skills, including program/project tasks coordination. Excellent verbal and written communications with business stakeholders and peers. Experience with GxP validation or other equivalent quality processes and documentation. Experience with vendor management as it relates to coordinating onsite integrator work. Deep knowledge in at least one of the following IT technology areas: Client Server applications, Data Analytics, IT Infrastructure, or Cyber Security. Desirable: Experience working in a validated manufacturing business environment. Experience with Power BI dashboard and report creation. SQL, Oracle, or other relational database experience. Person Brief: Bachelor’s degree in Computing, IT, Data Analytics, Engineering, or a highly related discipline. 1 year plus experience working in a relevant IT focused role where the above experience has been gained. Ideally, this will be within a manufacturing focused business. Strong analytical, troubleshooting, written & verbal communication skills are essential. The role is based onsite in Donegal, so you must be living in the area or able to relocate in a short time frame and be able to be onsite daily. Opportunity Brief: This is an excellent opportunity to work with clients who are global leaders in their field, helping to develop and improve upon industry-leading technology solutions. NNIT Ireland offers a supportive environment committed to employee development and wellness, along with a competitive and rounded compensation package, which rewards high performers. Company Brief: NNIT Ireland are experts in the area of Equipment System Integration and System Support. We specialize in assisting our customers, including many of the world’s top multinational companies in the medical device and pharmaceutical sectors, achieve their Six Sigma and OEE targets. Over the past 20 years, we have grown our business from a Sligo-based enterprise into an international business with additional offices in Galway, Limerick, Leinster, and Florida USA. We pride ourselves on our expertise in industrial IT integration and regulatory compliance in support of global end users, OEMs, and Technology providers. #J-18808-Ljbffr

  • Senior Automation Systems Engineer  

    - Kilkenny

    The Role: Senior Automation Systems Engineer Kilkenny Hybrid role - Typically 3 days onsite per week will be required but for the right candidate there is some room for flexibility Permanent or Contractor Role Brief: The role will focus on the development of an OEE system for using OSI Pi that will connect to production lines through Kepware OPC. The principal task will be to ensure the correct PLC data is available to generate the required OEE reports and dashboards. Responsibilities: Define the PLC data needed for OEE. Review PLC code from vendors (mixture of Rockwell ControlLogix and SoftPLCs written in structured text) and do a gap analysis in data requirements. Troubleshoot any connection issues between PLC tags and Kepware. Work with OSI Pi developer on any PLC related topics. Design code changes to generate any missing data from PLCs. Work with OEM vendor controls engineers, as appropriate, to develop and test code changes. Write change requests/change impact assessments to gain approval for implementing code changes. Manage implementation of code changes. Preferred Technical Skills: Expert knowledge on PLC programming ideally with Rockwell systems. Strong experience in the implementation of coding changes. Knowledge of OSI Pi systems integration with PLC systems. Strong understanding of PLC data extraction and capabilities. Experience in generation / execution of software test plans. Experience in FAT, SAT, commissioning & validation of high-speed automation equipment. Person Requirements: Bachelor's degree in Industry Automation, Mechatronics, Computer science, Electrical engineering or equivalent technical experience and demonstrated competence. 5+ years automation systems engineering experience with at least 3 years in a Life Sciences or Pharmaceutical manufacturing environment and a strong understanding of GMP standards and regulations. Strong communication skills and stakeholder management skills. Exceptional attention to detail. The role is based in Kilkenny and ideally you can do at least 3 days a week onsite. However for the right candidate with strong and relevant experience some flexibility around the onsite requirement is possible. You should be living within a reasonable commute of the site location or able to relocate and commence employment within 1 month maximum. Opportunity Brief: This is an excellent opportunity to work with clients who are global leaders in their field, helping to develop and improve upon industry leading technology solutions. SL Controls offer a supportive environment committed to employee development and wellness, along with a competitive and rounded compensation package, which rewards high performers. Company Brief: SL Controls are experts in the area of Equipment System Integration and System Support. We specialise in assisting our customers, including many of the world’s top multinational companies in the medical device and pharmaceutical sectors, achieve their Six Sigma and OEE targets. Over the past 20 years we have grown our business from a Sligo based enterprise into an international business with additional offices in Galway, Limerick, Leinster and Florida USA. We pride ourselves on our expertise in industrial IT integration and regulatory compliance in support of global end users, OEM’s and Technology providers. Find out more about working at SL Controls , our Sustainable Development Goals , and our Diversity, Equity, and Inclusion policy . #J-18808-Ljbffr

  • Lead Automation Engineer  

    - Kilkenny

    The Role: Lead Automation Engineer Kilkenny Onsite role - the role is designated onsite and the chosen candidate must be available to be onsite daily Permanent or Contractor opportunity Role Brief: SL Controls require a Lead Automation Engineer to supervise and lead a team of graduate and junior engineers working across a variety of shifts for a key client. The role will focus on the development of an OEE system for using OSI Pi that will connect to production lines through Kepware OPC. The Lead Automation Engineer's task will be to ensure the supervision and guidance of a team of engineers whose principal task will be to ensure correct PLC data is available to generate the required OEE reports and dashboards. Responsibilities: Supervise and guide a team of engineers Mentor and develop engineers to ensure strong levels of service delivery and continuous improvement Assist with defining the PLC data needed for OEE. Supervise the review of PLC code from vendors (mixture of Rockwell ControlLogix and SoftPLCs written in structured text) and do a gap analysis in data requirements. Troubleshoot any connection issues between PLC tags and Kepware. Collaborate with OSI Pi developer on any PLC related topics. Design code changes to generate any missing data from PLCs. Work with OEM vendor controls engineers, as appropriate, to develop and test code changes. Write change requests/change impact assessments to gain approval for implementing code changes. Manage implementation of code changes. Preferred Technical Skills: Senior or lead Automation Engineer experience Expert knowledge on PLC programming ideally with Rockwell systems. Significant experience in the implementation of coding changes. Knowledge of OSI Pi systems integration with PLC systems. Strong understanding of PLC data extraction and capabilities. Experience in generation/execution of software test plans. Experience in FAT, SAT, commissioning & validation of high-speed automation equipment. Person Requirements: Bachelor's degree in Industry Automation, Mechatronics, Computer Science, Electrical Engineering or equivalent technical experience and demonstrated competence. 7+ years automation systems engineering experience with at least 3 years in a Life Sciences or Pharmaceutical manufacturing environment and a strong understanding of GMP standards and regulations. Senior or lead engineer level experience with exposure to leading and mentoring more junior engineers Strong project management and project delivery skills and experience Exceptional communication and stakeholder management skills. Exceptional attention to detail. The role is based in Kilkenny and is designated as onsite so you must be available to be onsite full time as required. Occasional remote working may be possible but full onsite availability is essential. You should be living within a reasonable commute of the site location or able to relocate and commence employment within 1 month maximum. Opportunity Brief: This is an excellent opportunity to work with clients who are global leaders in their field, helping to develop and improve upon industry-leading technology solutions. SL Controls offer a supportive environment committed to employee development and wellness, along with a competitive and rounded compensation package, which rewards high performers. Company Brief: SL Controls are experts in the area of Equipment System Integration and System Support. We specialise in assisting our customers, including many of the world’s top multinational companies in the medical device and pharmaceutical sectors, achieve their Six Sigma and OEE targets. Over the past 20 years we have grown our business from a Sligo-based enterprise into an international business with additional offices in Galway, Limerick, Leinster and Florida USA. We pride ourselves on our expertise in industrial IT integration and regulatory compliance in support of global end users, OEMs and Technology providers. #J-18808-Ljbffr

  • The Role: IT Applications Specialist Donegal Onsite Role Contractor role Role Brief: The IT Applications Specialist will have primary responsibility for the IT Support effort of the Manufacturing Execution System (MES) - POMSnet & all auxiliary systems. You will play a key role in managing the site's overall IT business objectives. The role will interface with all areas of the business & participate in all aspects of the manufacturing through implementation & day-to-day support. Core Responsibilities: Monitors IT processes to ensure compliance with corporate, divisional and local policies and procedures. Support IT maintenance schedules. Support the site, critical manufacturing systems, interface with the business, assist with change control documentation and participate in testing schedules, delivery and testing coordination. Supports system software upgrades including planning and scheduling & testing with operations. Ensures policies and standards adherence is consistent with Corporate/Division standards. Supports and enforces audit compliant policies and standards. Ensures Local IT has business continuity/disaster recovery plans and participates in testing of plans as necessary and monitors results of business continuity testing. Act as the primary liaison between the IT and business areas, supporting applications in areas such as Manufacturing Execution Systems (MES), Labelling, and general manufacturing control systems. Skills Brief: Experience working with operating procedures, policies and processes in a GMP environment - Pharma/Life Sciences or Medical Devices. Candidates without this experience cannot be considered. Ability to investigate/troubleshoot MES and control systems to support optimization of system operations. Ability to assist with new machine integrations, configurations & peripheral devices setups. Exposure to supporting large scale Oracle upgrade implementation, preferable. Experience with ERP systems POMSnet & integrations with applications such as SAP, OSI-PI, Kepware advantageous. Experience in Oracle Databases, SQL scripting, Label printers, Scanners Configurations. Experience with Software Lifecycle Validations in a regulated industry is desirable. Person Brief: Bachelor’s degree in Computing or equivalent in Manufacturing or Engineering discipline. 3 years plus experience working in IT/MES environment preferably with direct manufacturing exposure. Strong analytical, troubleshooting, written & verbal communication skills are essential. The role is based onsite in Donegal so you must be living in the area or able to relocate in a short time frame and be able to be onsite daily. Opportunity Brief: This is an excellent opportunity to work with clients who are global leaders in their field, helping to develop and improve upon industry leading technology solutions. NNIT Ireland offers a supportive environment committed to employee development and wellness, along with a competitive and rounded compensation package, which rewards high performers. Company Brief: NNIT Ireland are experts in the area of Equipment System Integration and System Support. We specialise in assisting our customers, including many of the world’s top multinational companies in the medical device and pharmaceutical sectors, achieve their Six Sigma and OEE targets. Over the past 20 years we have grown our business from a Sligo based enterprise into an international business with additional offices in Galway, Limerick, Leinster and Florida USA. We pride ourselves on our expertise in industrial IT integration and regulatory compliance in support of global end users, OEMs and Technology providers. #J-18808-Ljbffr

  • Project Manager - MES  

    - Dublin

    The Role: Project Manager - MES Hybrid. The role will require onsite presence in Cavan for set activities and as required. Remote working is possible for other activities but you therefore must be based in Ireland and able to commute onsite as required. Ireland - Site location is County Cavan. Contract or Permanent Opportunity Role Brief: The successful candidate will lead and manage the implementation of a new MES solution, ensuring alignment with business objectives, timelines, and quality standards. You will oversee platform projects focused on enhancing and optimizing existing MES systems, driving innovation and operational efficiency. Core Responsibilities: Lead and manage the implementation of a new MES solution. Manage critical support initiatives for MES applications, ensuring timely issue resolution, system maintenance, and continuous improvements. Guide and coordinate cross-functional teams to successfully execute MES implementations, platform projects, and support initiatives. Demonstrate expertise in both waterfall and agile project management methodologies, adapting approaches based on project needs. Collaborate closely with stakeholders, end-users, and external partners to gather requirements, define project scope, and drive successful outcomes. Identify, assess, and mitigate project risks related to MES implementation, platform enhancements, and support efforts. Establish and enforce quality control processes to ensure the delivery of high-quality MES solutions and support services. Optimize project resources, including internal team members and external contractors, to maximize efficiency and ensure success. Provide regular project status updates to key stakeholders, communicating progress, challenges, and scope changes effectively. Lead continuous improvement initiatives within MES project management processes to enhance overall effectiveness. Skills Brief: Bachelor’s degree in a relevant field; Master’s degree or certifications (PMP, Agile, etc.) preferred. Minimum of 3 years of experience managing IT projects in a GMP environment, with a focus on MES implementations. Strong knowledge of both waterfall and agile project management methodologies. Excellent communication, leadership, and interpersonal skills. Proven ability to deliver projects on time, within budget, and with a strong focus on quality. Experience in medical devices / pharmaceutical manufacturing industries. Person Brief: Candidates must have a level 8-degree qualification with a minimum of three years’ relevant industry experience in medical devices, pharmaceutical or biotechnology manufacturing environments. The ideal candidate will have excellent collaboration and communication skills, with the ability to work in a fast-paced, dynamic environment. In addition to this, strong attention to detail, including the ability to proofread documents and to accurately translate customers’ requirements into meaningful end-user instructions consistently is required. You should have a mix of strong and relevant technical skills and proven client and project management skills. Ideally, you will have 3-5 years experience in project managing projects in a GMP environment. A PMP / Prince / PgmP Certification is highly advantageous. The candidate should be based in Ireland and able to travel onsite to Cavan as required. While remote working will be possible for some tasks and functions, the role is not possible to undertake fully remote and you will be required to be onsite at least a number of days per month or as per project requirements. Opportunity Brief: This is an excellent opportunity to work with clients who are global leaders in their field, helping to develop and improve upon industry-leading technology solutions. NNIT Ireland offers a supportive environment committed to employee development and wellness, along with a competitive and rounded compensation package, which rewards high performers. Company Brief: NNIT Ireland are experts in the area of Equipment System Integration and System Support. We specialise in assisting our customers, including many of the world’s top multinational companies in the medical device and pharmaceutical sectors, achieve their Six Sigma and OEE targets. Over more than 20 years we have grown our business from a Sligo-based enterprise into an international business with additional offices in Galway, Limerick, Leinster, and Florida USA. We pride ourselves on our expertise in industrial IT integration and regulatory compliance in support of global end users, OEMs, and Technology providers. #J-18808-Ljbffr

  • Senior Project Lead  

    - Limerick

    The Role: Senior Project Lead Limerick Onsite role Permanent or Contractor Opportunity Role Brief: The Senior Project Lead will be responsible for managing complex end-to-end projects for an NNIT Ireland client. You will work closely with a variety of stakeholders to align project objectives with organizational goals and drive continuous improvement in project management processes. Core Responsibilities: Lead the planning and implementation of projects, ensuring alignment with business objectives. Define project scope, goals, and deliverables in collaboration with senior management and stakeholders. Develop detailed project plans, schedules, and budgets, and manage resources effectively. Build, lead, and motivate cross-functional project teams. Assign tasks and responsibilities to team members and ensure accountability. Serve as the primary point of contact for project stakeholders. Communicate project status, risks, and issues to stakeholders and senior management. Manage stakeholder expectations and ensure alignment with project goals. Identify potential project risks and develop mitigation strategies. Prepare and present project reports and documentation to stakeholders and senior management. Maintain comprehensive project documentation throughout the project lifecycle. Skills Brief: Requires BS/BEng in Chemical, Process, or Mechanical engineering with 7 - 10 years related experience in project management, with a proven track record of leading complex projects. Direct experience of over 3 years with biopharmaceutical process equipment is a definite requirement. GMP and GDP environment experience is essential. Proven working experience as a Project Manager. Project Management Professional (PMP) certification or equivalent is required. Strong leadership and team management skills. Excellent communication, negotiation, and interpersonal skills. Proficiency in project management software and tools. Person Brief: The ideal candidate for this role will be an experienced and certified Project Manager who has delivered complex projects in manufacturing environments. It is essential you will have 3 or more years’ experience in GMP/GDP environments (Biopharma, Life Sciences, Pharma). You should be very comfortable managing multiple projects simultaneously and have excellent stakeholder and vendor management skills allied to first-class communication skills across all forms of communication. The role is based in Limerick and will be mostly onsite so you should be willing and able to commute daily to site and therefore you must currently be living within a reasonable commute of the site or able to relocate in a 1 to 2 month period. Opportunity Brief: This is an excellent opportunity to work with clients who are global leaders in their field, helping to develop and improve upon industry-leading technology solutions. NNIT Ireland offers a supportive environment committed to employee development and wellness, along with a competitive and rounded compensation package, which rewards high performers. #J-18808-Ljbffr

  • The Role: Senior Siemens Systems Automation Engineer Onsite Role - No remote working. The role is fully onsite. Sligo Permanent or Contractor Role Brief: The successful candidate will be responsible for the development, commissioning, and support of automation and control systems. You will also handle the design, specification, programming, simulation, testing, and start-up assistance for these systems. You must have strong experience working with Siemens and possess the technical expertise to maintain, develop, troubleshoot, and validate these systems in a compliant manner. Skills Brief: 10+ years experience working with Siemens PLC Systems Proven knowledge and experience with one or more of the following will be an advantage: SCADA, Control Systems, Vision Systems Pack equipment systems, Cognex and Serialization experience – Some level of experience in all or any of these is highly advantageous Strong exposure to automation systems integration, solution design, in life sciences or medical devices is essential Experience in implementation and troubleshooting of SQL database systems for real time process data collection is an advantage. IT/Networking experience would be advantageous High level languages experience would be advantageous Person Brief: Candidates must have a B.Sc. Degree in Engineering or equivalent, with emphasis in software development, electrical, electronic or automation discipline, with a minimum of 10 years’ experience in industry, preferably in a pharmaceutical, biotechnology, blue chip or relevant GMP manufacturing environment. The ideal candidate will have excellent communication & problem solving skills as well as strong stakeholder & vendor management skills. As this role is fully onsite in Sligo, the successful candidate must be based in Sligo or within a reasonable commute. Only candidates with a current valid work permit to work in Ireland can be considered due to project timelines. Opportunity Brief: This is an excellent opportunity to work with clients who are global leaders in their field, helping to develop and improve upon industry leading technology solutions. NNIT Ireland offers a supportive environment committed to employee development and wellness, along with a competitive and rounded compensation package, which rewards high performers. Company Brief: NNIT Ireland are experts in the area of Equipment System Integration and System Support. We specialize in assisting our customers, including many of the world’s top multinational companies in the medical device and pharmaceutical sectors, achieve their Six Sigma and OEE targets. Over the past 19 years we have grown our business from a Sligo based enterprise into an international business with additional offices in Galway, Limerick, Leinster and Florida USA. We pride ourselves on our expertise in industrial IT integration and regulatory compliance in support of global end users, OEM’s and Technology providers. SL Controls provides Equipment System Integration solutions to manufacturers, particularly those in the life sciences and technology sectors. Due to the ongoing growth and expansion of our business, we have a number of exciting engineering career opportunities available. The roles are based in various locations across Ireland as well as in our office in the USA. Our engineers deliver cutting-edge Smart Factory and Industry 4.0 solutions, so the work is rewarding and challenging. We also offer excellent opportunities for career progression. #J-18808-Ljbffr

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