Seeking a Senior Quality Engineer to support Quality aspects impacting the successful functioning of a manufacturing facility, with a focus on developing and implementing solutions to sustain and improve the QMS. Key Responsibilities Develop and implement solutions to sustain and improve the QMS. Maintain and support compliance to required regulated systems standards. Interface with customers on new products, quality issues and process qualifications. Develop and implement process control programs to ensure customer requirements are met. Carry out process validations and qualification on products. Provide manufacturing support and quality expertise in relation to manufacturing issues and product disposition. Perform quality engineering analysis to identify strategies to prevent quality nonconformances and minimize risk. Coordinate NCMR / CAPA Process to ensure timely resolution and closure of issues. Lead training activities on Quality Procedures, e.g., Compliance, GMP, Audit Prep and GDP. Support and represent the site during external audits and carry out Internal Audits. Support Environmental, Health and Safety requirements, training, and regulations. Requirements Third level qualification in Engineering, Quality, Validation, or equivalent Manufacturing experience. Knowledge of CAPA's, NCMR's, Change Controls and SCAR's from a Quality perspective. Experience in statistical analysis (Minitab) / SPC / validations. Excellent interpersonal, communication, influencing, and facilitation skills. A minimum of 3 years' experience as a Quality Assurance Engineer within medical device or pharmaceutical manufacturing environment. About the Company SL Controls are experts in the area of Equipment System Integration and System Support, assisting clients in achieving their Six Sigma and OEE targets. We pride ourselves on our expertise in industrial IT integration and regulatory compliance in support of global end users, OEM's and Technology providers.
Senior Validation Engineer role in Galway, Ireland, involves leading the Validation Program, including Computer Systems Validation and Quality Assurance activities, with a focus on equipment, utilities, processes, and software. The Role Senior Validation Engineer Galway, Ireland Hybrid role with some remote working possible Permanent or Contractor Role Responsibilities Lead the Validation Program, including Computer Systems Validation and Quality Assurance activities Coordinate and direct the validation and qualification of equipment, utilities, processes, and software Ensure conformance to quality systems and liaise with various departments Review documentation and ensure adherence to company validation policies and procedures Generate and maintain project validation plans and schedules Develop and execute validation protocols and final reports to cGMP standards Provide QA support for validation investigations and implementation of corrective actions Manage validation, exception event, and change control processes Document all activities in line with cGMP requirements Perform cross-training within the team and train new team members Participate in continuous improvement programs to implement improvements in manufacturing, quality, safety, and training systems Requirements Relevant science or engineering tertiary qualification Minimum 5 years' experience in the pharmaceutical or life sciences industry Strong experience of General and Computer Systems Validation (CSV) Experience in Equipment & Process Validation beneficial Experience of GxP Computerised Systems and GAMP 5 essential Excellent collaboration and communication skills Demonstrated understanding of manufacturing processes and related process equipment Strong attention to detail and understanding of validation concepts and documentation About the Company SL Controls is a global leader in the development and improvement of industry-leading technology solutions, offering a supportive environment committed to employee development and wellness, and a competitive and rounded compensation package.
The Role: Business Operations Associate Remote (Based in Ireland) - Occasional travel required but not significant Fixed Term Contract (FTC) - 12 months Role Brief: As Business Operations Associate, you will be part of the commercial team and are responsible for supporting the defined strategy with a focus on achieving and exceeding quarterly and annual targets in line with the overall company targets and objectives. You will work closely with the Commercial Management Team to support business growth strategies. You are expected to support the growth of the SL Controls/NNIT brand through tailored marketing initiatives with the objective of generating increased awareness of SL Controls core services to existing and new clients. You will help ensure that a company culture of respect, dignity and continuous improvement is fostered for all employees in order to promote personal and career development in conjunction with the achievement of the overall company goals. You are expected to maintain personal productivity and quality standards that make possible targeted financial returns so that the company may continue to provide our excellent service to our customers and ensure job security and career growth for our employees. Key Responsibilities: Support the overall commercial strategy implementation to open client accounts and further penetrate existing client accounts in both Ireland and abroad that require project and contract staffing solutions. Monitor client KPI’s that are delivered directly to client representatives at consistent intervals during the calendar year. Demonstrate initiative on identifying areas for improvement within the commercial department. An emphasis on continual improvement within the department is essential for ensuring that SL Controls continues to be at the forefront on winning and maintaining business with new and existing clients at national and international levels. Support and have key input into the generation of a coordinated marketing plan that encompasses all aspects of SL Controls service offerings. This is a key activity that will facilitate a coordinated and consistent message to existing and prospective clients. Coordinate with the marketing department and be involved in the key aspects of social media in order to drive the SL Controls brand and be up to date on market and competitor activity. Active involvement in key events or conferences that drive the business forward. Prepare sales proposals to meet with client expectations whilst also ensuring that proper adherence is given to achieving headline financial target margins. Present & manage the agreed KPI information to the Commercial Department at agreed intervals. Involvement in the creation, review and approval cycle of commercial related documents. Update job knowledge by participating in educational opportunities; reading professional publications; maintaining personal networks; participating in professional organizations. Conduct market research and analysis of competitor activities. Support the management of the CRM systems within the SL Controls/NNIT business and manage and lead the associated activities. Skills Brief: The ideal candidate for this role will have the following skills: Preference will be given to candidates from an Engineering background but we will also consider business/commerce graduates with a good technical competency. Excellent communication, presentation and negotiation skills. Exceptional organisational and planning skills. Experience selling services from initial contact through to contract closure. Familiarity with CRM software such as Salesforce/HubSpot/Microsoft Dynamics. Demonstrated success in consistently exceeding sales goals and targets. Preferable to have 1 or more years’ experience in a similar role. Person Brief: The ideal candidate will be a recent graduate with at least 1 year of post-graduate or undergraduate internship experience in a commercially focused role. You should be able to collaborate with other key internal stakeholders to drive the business forward and achieve your goals. You must combine these qualities with strong organizational skills and, particularly, a keen eye for detail. While this role is remote you must be available to travel circa 2 days per week to office or customer locations. Candidates will ideally have a full clean driving license and their own car (mileage will be paid for work-related travel). 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
The Role Senior Quality Engineer Athlone Hybrid role with some remote working possible Permanent or Contractor Role Role Brief Reporting to the Quality Manager you will be responsible for supporting all Quality aspects impacting the successful functioning of the manufacturing facility. Main responsibilities: Developing and implementing solutions to sustain and improve the QMS. Maintain and support compliance to required regulated systems standards. Interface with customers on new products, quality issues and process qualifications. Develop and implement process control programs to ensure customer requirements are met. Carry out process validations and qualification on products. Provides manufacturing support and quality expertise in relation to manufacturing issues and product disposition. Performing quality engineering analysis to identify strategies to prevent quality nonconformances and minimize risk. Co-ordinate NCMR / CAPA Process to ensure timely resolution and closure of issues. Lead training activities on Quality Procedures, e.g., Compliance, GMP, Audit Prep and GDP. Supporting and representing the site during external audits and carrying out Internal Audits. Supporting Environmental, Health and Safety requirements, training, and regulations. Skills Brief Third level qualification in Engineering, Quality, Validation, or equivalent Manufacturing experience. Knowledge of the following from a Quality perspective – CAPA’s, NCMR’s, Change Controls and SCAR’s. Experience in statistical analysis (Minitab) / SPC / validations. Excellent interpersonal, communication, influencing, and facilitation skills. A minimum of 3 years’ experience as a Quality Assurance Engineer within medical device or pharmaceutical manufacturing environment. Person Brief Third level qualification in Engineering, Polymer Science, Biotech or equivalent Pharma or Medical Device manufacturing experience. A minimum of a level 8 Degree qualification. 2 years experience in a Quality / Validation role in a Pharma or Medical Device manufacturing environment. Living within a reasonable commute of the Athlone site location and with suitable transport enabling you to be onsite at least 50% of the time. 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. #J-18808-Ljbffr
The Role Senior Validation Engineer Galway Hybrid role with some remote working possible Permanent or Contractor Role Role Brief The successful candidate will have a senior level of responsibility for the Validation Program including Computer Systems Validation (CSV) and general Quality Assurance activities. You will also have responsibility for the coordination and direction and active participation in the validation and qualification of equipment, utilities, processes and software. You will be responsible for ensuring conformance to quality systems, liaising with various departments, giving guidance, reviewing documentation and ensuring the company validation policies & procedures are being adhered to. Skills Brief Active participation in the Validation Program and general Quality Assurance activities. Validation of a range of computer systems Coordination / direction and active participation in the validation and qualification of equipment, utilities, processes and software in compliance with client policies, FDA, European cGMP and GAMP standards. Generation/maintenance/execution of Project Validation Plans and schedules. Generation of validation protocols and final reports to cGMP standards. QA support for validation investigations and implementation of corrective actions. Creation/Review/Approval of various validation and qualification documents. Management of validation, exception event, and change control processes. Documenting all activities in line with cGMP requirements. Performing cross training within the team and training of new team members. Participation in continuous improvement programs to implement improvements in manufacturing, quality, safety and training systems. Person Brief Candidates must have a relevant science or engineering tertiary qualification with a minimum of 5 years’ experience in the pharmaceutical or life sciences industry with strong experience of both General and Computer Systems Validation (CSV). Experience in Equipment & Process Validation would also be beneficial. Experience of GxP Computerised Systems and GAMP 5 is essential. The ideal candidate will have excellent collaboration and communication skills, with a demonstrated understanding of manufacturing processes and related process equipment. In addition to this, strong attention to detail and an excellent understanding of validation concepts and documentation is required. The role will be based in Galway and is hybrid with some remote working possible. You should be living within a reasonable commute of the Galway area and be available to be onsite as required which could be up to 5 days a week at times. 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. #J-18808-Ljbffr
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. The Role: Project Engineer Dublin Onsite role - Remote working is very limited with this role and therefore you should be living in or close to Dublin to be able to commute to the site as required. Permanent or Contractor Opportunity Role Brief: The Project Engineer is responsible for coordinating, managing the design, installation and operational start-up of new systems/equipment or system upgrades. You will be responsible for project planning and delivery around new projects, systems changes and upgrades of systems. Core Tasks: To coordinate and manage the design, installation and operational start-up of new systems/equipment or system upgrades. To ensure that any system or equipment introduced under an assigned project is handed over to the end user to include transfer of knowledge, necessary training and ongoing requirements if applicable. Work with external suppliers/sub-contractors to acquire components, materials, and/or equipment that meet client requirements and user requirements. To manage sub-contractors or service providers in the execution of support activities/testing on site in accordance with client requirements. To work with and coordinate cross-functional teams for optimum project delivery and ensure project needs and outcomes are communicated accordingly. To proactively resolve project challenges and where necessary escalate any issues to ensure the correct support and resources are allocated to resolve any issues foreseen or that occur during project implementation. To provide Engineering support for Non-Conformance Investigations. Implement CAPA Actions and Change Plan Tasks as needed. To work with external vendors and suppliers and review design and handover packages/supporting documentation/test packs/protocols to ensure they meet the end need of the user, client requirements and any applicable Engineering standards. Skills Brief: Minimum of 3 years' experience in a similar role delivering projects in Pharma, Life Science of Medical Device (GMP) manufacturing environments. Clear understanding of a range of automation systems technologies, regulations and standards. Proven track record in a project delivery focused role in the above industry sectors. Project engineering skills including budgeting, vendor management, and the generation, execution and approval of Qualification Life Cycle Documentation. Experience in commissioning and qualification of projects of low, medium and major complexity. A strong understanding of relevant standards and regulations such as ISO. Person Brief: Candidates must have a level 8-degree qualification with a minimum of 3 years’ relevant industry experience in pharmaceutical, biotechnology or medical device 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 accurately translate customers’ requirements into meaningful end-user instructions consistently is required. You should have a mix of relevant technical skills and knowledge as well as proven client and project management skills. The candidate should be based in or near Dublin and able to travel onsite to the site daily as this is an onsite role. 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, OEMs 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
The Role Senior Commissioning and Qualification Engineer Sligo Onsite role – no remote working so you must be living within a reasonable commute of the Sligo site Permanent or Contract Role Brief The successful candidate will work within the Engineering department with a key SL Controls client. The role reports into the Senior Process Engineer and will have responsibility for the generation, execution and approval of a range of Qualification Life Cycle documents from SLIA through to PQ and Final Summary Reporting for Direct Impact Systems. Core Responsibilities: Generation, Execution / Approval of Qualification Life Cycle documents from SLIA through to PQ and Final Summary Reporting for Direct Impact Systems. Generation of Commissioning Test documents for No Impact Systems. Implementation of Change Controls on the change management system to support project activities as applicable. Coordination and management of all elements of commissioning & qualification of large and small scale projects. Developing a project plan and qualification strategy in line with client requirements. Coordinate and supervise third party suppliers / vendors, service providers and sub-contractors as necessary. Monitor and report on project plan progress, communicate any shortfalls in specific areas of the plan and identify solutions to address the shortfalls. Participate in decision forums to decide on priorities and ensure these are reflected in the plan, schedule and communications. Evaluate allocation of resources needed to complete project tasks and provide recommendations to maintain required progress. Monitor budgets closely reporting on funding committed, expenditure forecasting and progress. Skills Brief Able to demonstrate a knowledge of Systems and Equipment and engineering design. 5 years’ experience in projects in the Pharmaceutical or Biotech/Medical devices sectors in a major project environment. Clear understanding of a range of automation systems technologies, regulations and standards. Proven track record in a project delivery focused role in the above industry sectors. Project engineering skills including budgeting, vendor management, and the generation, execution and approval of Qualification Life Cycle Documentation. Experience in commissioning and qualification of projects of low, medium and major complexity. Person Brief Candidates must have a B.Sc. degree in Engineering or equivalent electrical, electronic or automation discipline, with a minimum of 5 years’ experience in a GMP manufacturing environment such as pharmaceutical, biotechnology or medical devices. The ideal candidate will have excellent communication skills and strong problem-solving skills. As this is an onsite role in Sligo you should be living within a reasonable commute and be able to attend the site daily or be able to relocate within 1 to 2 months 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
The Role Senior Automation Engineer Sligo Onsite role Permanent or Contractor Role Brief As a Senior Automation Engineer you will be responsible for providing subject matter expect software support for wide ranging manufacturing processes. You will participate in design, planning and support of the introduction of high-speed automation lines. This role provides technical leadership in areas of PLC communications, vision and RFID communications while driving activities at the supplier(s) to ensure automation & software support is achieved. You will direct the works of technical, validation and less experienced engineering staff and will also interface with product team members, department managers, designers/equipment manufacturers, R&D, quality, and regulatory personnel. Responsibilities: Control and implement any relevant engineering changes. Independently conceive and develop approaches to the solution of problems which require application of advanced technical knowledge – applies working knowledge of related disciplines. Solve problems with a variety of complex features such as conflicting design requirements, unsuitability of conventional materials and difficult coordination requirements. Independently design and lead complex engineering studies and experiments often with multiple variables. Analyse complex problems and identify their impact as well as establish probabilities. Draw conclusions reflecting broad business needs. Set complex design and process requirements. Complete documentation in a timely manner and in accordance with business standards. Lead and/or participate on technical cross-functional teams to support organizational goals. Understand and comply with applicable EHS policies, procedures, rules and regulations. Other tasks and duties as assigned Skills Brief Expert knowledge on PLC programming with Allen Bradley/Siemens/Codesys controls systems. Expert knowledge of Cognex vision systems. Working knowledge of RFID communications. Experience in generation / execution of software test plans. Experience in FAT, SAT, commissioning & validation of high-speed automation equipment Person Brief Bachelor’s degree in Industry Automation, Mechatronics, Computer science, Electrical engineering or equivalent technical experience and demonstrated competence. 4+ years of experience in an automation engineering role with at least 2 years of this in Good Manufacturing Practice (GMP) environments (Life Sciences, Pharma, Medical Devices). Based in the Sligo area or within a reasonable commute and able to be onsite daily as the role does not offer remote working. 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
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. The Role: Senior Automation Engineer Location: Limerick Type: Onsite role, 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 be responsible for automation and control systems design, specification, programming, simulation, testing, and start-up assistance. In this role, you will be required to work closely with Vendors and OEMs to deliver the optimum solution for the client in a vendor package capacity. The candidate must possess the technical expertise to maintain, develop, troubleshoot, and validate these systems in a compliant manner. Skills Brief: Must have strong experience with either Allen Bradley or Siemens (Step7) PLC Systems but familiar with both platforms. 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 but subject matter expert level experience is NOT required Experience in the validation of automated processes for pharmaceuticals. Experience in implementation and troubleshooting of SQL database systems for real-time process data collection is an advantage. IT/Networking 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 5 years’ experience in industry, preferably in a pharmaceutical, biotechnology, blue chip, or relevant GMP manufacturing environment. The ideal candidate will have excellent communication skills and strong problem-solving skills. 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, OEMs, 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
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. Skills Brief 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 Brief 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. Ideally living within a reasonable commute of Kilkenny 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. #J-18808-Ljbffr
