Réalta Technologies are searching foranMES Engineer to join our team, supporting a prominent pharmaceutical client’s manufacturing operations. This role is focused on the configuration, deployment, and support of the Manufacturing Execution System (MES), specifically in the areas of column packaging, media preparation, and buffer preparation. The ideal candidate will play a key role in enhancing manufacturing processes, ensuring data integrity, and supporting end-to-end production throughPAS-X MES. Key Responsibilities PAS-X Configuration & Support: Configure, deploy, and maintain PAS-X MES to support manufacturing processes, including column packaging, media, and buffer preparation. Process Optimization: Collaborate with production and engineering teams to analyze and optimize MES-related workflows for efficiency, accuracy, and regulatory compliance. Documentation & Validation: Develop, review, and maintain system documentation, including user requirements, functional specifications, SOPs, and validation protocols, in line with GxP standards. Troubleshooting & Technical Support: Provide day-to-day MES support to end users, addressing system issues, troubleshooting errors, and implementing corrective actions. System Upgrades & Enhancements: Assist in system upgrades, testing, and the rollout of new PAS-X features or modules, ensuring minimal impact on operations. Training & Knowledge Transfer: Train production staff on MES functionalities and provide ongoing support to ensure effective use of the system. Compliance & Quality Assurance: Ensure all activities comply with relevant regulatory and quality standards, including GMP, FDA, and GAMP5 guidelines. Qualifications Bachelor's degree in Engineering, Computer Science, Information Technology, or related field. Minimum of 3-5 years of experience as an MES Engineer, preferably in a pharmaceutical or biotech environment. Hands-on experience with PAS-X MES system is essential. Proficiency in PAS-X MES configuration, customization, and troubleshooting. Strong understanding of pharmaceutical manufacturing processes, especially around column packaging, media preparation, and buffer preparation. Knowledge of GxP, GMP, FDA, and other regulatory requirements in the pharmaceutical industry. Excellent problem-solving skills with a proactive approach to troubleshooting. Strong communication skills and ability to work effectively with cross-functional teams. Detail-oriented, with a strong commitment to documentation and quality. #J-18808-Ljbffr
Réalta Technologies is seeking a highly skilled Automation Engineer to join our team in Dublin. The ideal candidate will have experience with Rockwell or Siemens systems and possess expertise in IFix. With a significant increase in projects planned for the upcoming year, we are looking for an additional team member to support our automation initiatives. This role will involve working on a portfolio of projects, overseen by the capital team. Responsibilities: Design, develop, and implement automation solutions using Rockwell or Siemens systems. Utilize expertise in IFix to implement automation and control strategies. Collaborate with cross-functional teams to understand project requirements and objectives. Develop and execute automation test plans to ensure system reliability and performance. Troubleshoot and resolve automation issues to minimize downtime and optimize productivity. Ensure compliance with industry standards and regulatory requirements. Document and maintain accurate records of automation processes, configurations, and changes. Provide technical support and training to end users as needed. Requirements: Proven experience as an Automation Engineer, preferably in a pharmaceutical or biotechnology industry. Expertise in Rockwell or Siemens systems (both is a bonus), including programming and troubleshooting. Proficiency in IFix, with a track record of successful implementation. Familiarity with industry standards such as GAMP and 21 CFR Part 11. Excellent problem-solving and analytical skills. Strong communication and interpersonal skills to collaborate effectively with cross-functional teams. Ability to work independently, prioritize tasks, and meet project deadlines. Flexibility to adapt to changing project requirements and multitask effectively. #J-18808-Ljbffr
Réalta Technologies are searching for a Lead Data Scientist to join our internal projects team to support our ongoing projects. This person will play a crucial role in analyzing and interpreting complex data from our various clients. This expertise will be essential in discovering valuable insights that will contribute to the development and improvement of their products. In this role, the successful candidate will blend data science methodologies with SQL development skills to create a comprehensive data-driven environment. Key Responsibilities: Design and Oversee ETL Pipelines : Lead the design, implementation, and optimization of Extract, Transform, Load (ETL) processes to ensure efficient and accurate data flow from various sources to analytical platforms. Data Analysis and Modeling : Conduct advanced data analysis and develop predictive and prescriptive models using Python, leveraging libraries like pandas, NumPy, scikit-learn, and TensorFlow. Database Management and Querying : Design and manage relational databases, write and optimize SQL queries for data extraction and transformation, and ensure database integrity and performance. Data Visualization and Reporting : Create interactive dashboards and insightful visualizations using Power BI to communicate findings and support data-driven decision-making across the organization. Project Management and Collaboration : Collaborate with cross-functional teams, including data engineers, business analysts, and stakeholders, to align data analytics projects with organizational goals and ensure timely delivery. Mentoring and Skill Development : Provide technical guidance and mentorship to junior data scientists, fostering skill development in Python, SQL, ETL processes, and analytics best practices. Continuous Improvement : Identify opportunities to enhance analytics workflows, tools, and strategies to improve data accessibility, analysis, and overall business impact. Qualifications: Bachelor’s or Master’s degree in Data Science, Computer Science, Statistics, Mathematics, or a related field. Minimum of 5 years of hands-on experience in data analytics, machine learning, or similar roles. Experience in Medical Device or Pharmaceutical industry a plus. Minimum of 2 years experience in team leadership or management roles required. Proven expertise in designing, implementing, and optimizing ETL pipelines for data integration and transformation across diverse data sources. Strong programming skills in Python, including experience with libraries such as pandas, NumPy, scikit-learn, and TensorFlow for data analysis and machine learning. Demonstrated ability to write and optimize complex SQL queries, manage relational databases, and ensure data quality and integrity. Hands-on experience creating interactive dashboards and visualizations in Power BI to translate data insights into actionable business decisions. A solid track record in designing and deploying predictive and prescriptive models to solve real-world business challenges. Experience leading and mentoring data teams, fostering a collaborative environment, and guiding junior data scientists in technical skill development. Strong project management capabilities, with excellent communication skills to collaborate with cross-functional teams and effectively present findings to stakeholders. #J-18808-Ljbffr
Réalta Technologies are searching for an Automation Engineer to support our client's biopharmaceutical production facility in Cork. The ideal candidate will have 1-3 years' experience as an Automation Engineer in the Life Sciences industry. Responsibilities Provide daily support for automation systems within the biopharmaceutical production facility. Ensure optimal performance and reliability of automation systems through regular monitoring and maintenance. Diagnose and resolve technical issues related to automation systems promptly to minimise production downtime. Perform updates and modifications to automation system designs and code to improve functionality and efficiency. Ensure that all updates are thoroughly tested and documented. Review and understand design documentation, ensuring that all automation code aligns with the specified requirements. Maintain accurate records of system changes and ensure compliance with industry regulations and company policies. Requirements Bachelor's degree in Electrical Engineering, Automation, Computer Science, or a related field. 1-3 years of experience in automation engineering, preferably within a pharmaceutical or biotechnology environment. Experience with DCS (DeltaV, Foxboro, 800xA, PCS7) is a plus but not required. Proficiency in PLC programming, HMI development and SCADA systems. Strong understanding of automation design principles, process control and instrumentation. Excellent troubleshooting skills. Effective communication skills, with the ability to understand and interpret design documents and relate them to code. #J-18808-Ljbffr
Réalta Technologies is a leading automation and digital system firm that specializes in delivering innovative solutions to clients in the life science industries. We are seeking a highly motivated DeltaV Automation Engineer to join our team, you will be responsible for designing, developing, and implementing control systems supporting a drug & development facility using DeltaV. You will work closely with the project team to ensure that the systems are integrated, tested, and commissioned to meet the project requirements. Responsibilities: Design and develop control system solutions for the project using DeltaV automation technology Work with the project team to ensure that the control systems are integrated, tested, and commissioned to meet the project requirements Provide technical support and guidance to the project team during the installation and commissioning phases Develop and maintain project documentation, including specifications, functional requirements, and test plans Participate in design and code reviews to ensure that project standards and best practices are followed Identify and mitigate technical risks and issues to ensure project success Maintain a high level of technical knowledge and expertise in DeltaV automation technology Qualifications: Bachelor's degree in engineering or related field 4+ years of experience in DeltaV automation engineering Strong knowledge of DeltaV automation technology, including configuration, programming, and troubleshooting Strong problem-solving skills and attention to detail Excellent communication and interpersonal skills Ability to work effectively in a team environment #J-18808-Ljbffr
We are seeking a Principal Manufacturing Engineer who will be responsible for leading manufacturing process improvements, optimizing production efficiency, and implementing advanced engineering solutions in a manufacturing medical devices environment. You will play a key role in strategic decision-making, mentoring junior engineers, and driving innovation in production technologies. Key Responsibilities: 1. Process Optimization & Innovation Develop and implement advanced manufacturing processes to improve efficiency, quality, and cost-effectiveness. Drive continuous improvement initiatives using Lean Manufacturing, Six Sigma, and Industry 4.0 technologies. Evaluate and integrate automation, robotics, and smart manufacturing techniques. 2. Technical Leadership & Strategy Lead cross-functional teams in process development, troubleshooting, and optimization. Collaborate with R&D, design, and production teams to ensure manufacturability of new products. Develop long-term manufacturing strategies aligned with business goals. 3. Quality & Compliance Ensure manufacturing processes comply with industry standards (ISO, FDA, GMP, AS9100, etc.). Conduct root cause analysis (RCA) and implement corrective actions for quality issues. Improve product reliability and production yield through data-driven decisions. 4. Equipment & Automation Management Oversee selection, installation, and maintenance of advanced manufacturing equipment. Lead automation initiatives, including robotics, CNC, and smart factory solutions. Develop predictive maintenance strategies to minimize downtime. 5. Mentorship & Training Mentor and train junior engineers and manufacturing teams. Establish best practices, documentation, and knowledge-sharing programs. Foster a culture of continuous learning and innovation within the organization. Skills & Tools Required: Bachelor's degree in manufacturing, Electrical Engineering, Automation, Computer Science, or a related field. Proven experience as a Manufacturing Engineer or similar. Advanced Manufacturing Technologies – CNC, robotics, additive manufacturing. Lean & Six Sigma Methodologies – Black Belt or Green Belt certification preferred. Process Simulation & Data Analytics – MATLAB, Minitab, Python, AI/ML for manufacturing. Design for Manufacturability (DFM) & Design for Assembly (DFA). Project Management – PMP Certification is a plus. #J-18808-Ljbffr
Réalta Technologies are searching for a Project Engineer to support the development, growth and delivery of a Portfolio of Projects for our Medical Device client based in Cork. These projects will involve the development and deployment of new products and process technologies to multiple manufacturing locations. Also, work to reduce the cost of existing products through collaboration with R&D and development of next generation process technologies and capabilities. PRINCIPLE ACCOUNTABILITIES: New Inspection Technologies; Execution and project management responsibility NPI and Tech development projects. Emerging Product Development Manage risk management and validation lifecycle for new process or process changes. Management of the Asset Lifecycle for new equipment (URS/RA/IQ/OQ/PQ). Influence innovative qualification methodologies to apply appropriate statistical and validation techniques based on failure model and overall risk. Operations Development of advanced manufacturing processes to lean guidelines. Conduct engineering studies to ensure compliance. Business Results. Customer & Marketplace focus. Collaboration & Teaming. Requirements Education Requirements: Degree in Engineering, Science or a related discipline. A minimum of 3-4 years previous engineering experience within a Medical Device manufacturing environment. Strong influencing skills - Excellent communication skills (written and oral). Problem solving skills – To assist in maintaining project progress and on design issues. Decision Making – Required to make decisions on technical and management issues. Degree of responsibility – Must be capable of managing and developing the team. Excellent Planning & Organizing Skills. Extent of Confidentiality - Discretion is essential in view of contact with outside parties, product development strategies & regulatory. #J-18808-Ljbffr
We are seeking a highly motivated and skilled Field Service Engineer to join our team supporting a large pharmaceutical client of ours based in Limerick. The successful candidate will be responsible for installing, calibrating, maintaining, and troubleshooting instrumentation systems at client sites. This role requires hands-on technical expertise, strong problem-solving skills, and a commitment to providing exceptional service. Responsibilities: Installation and Commissioning : Install and commission instrumentation systems, ensuring they meet operational requirements and specifications. Calibration and Maintenance : Perform routine calibration, testing, and maintenance of sensors, transmitters, controllers, and other instrumentation devices. Troubleshooting and Repairs : Diagnose and resolve technical issues in instrumentation systems, minimizing downtime and ensuring optimal performance. Documentation : Maintain accurate records of service activities, including calibration reports, service logs, and recommendations for improvements. Customer Training and Support : Provide training and technical support to clients, ensuring proper use and understanding of installed systems. Compliance and Safety : Ensure all work complies with industry standards, company policies, and safety regulations. Requirements: Educational Background : Diploma or degree in Instrumentation, Electrical Engineering, or a related field. Experience : 3+ years of field experience in instrumentation, including installation, calibration, and troubleshooting. Technical Knowledge : Strong understanding of process control systems, sensors, transmitters, and related instrumentation technologies. Problem-Solving Skills : Excellent analytical skills with the ability to diagnose and resolve complex instrumentation issues. Travel Flexibility : Willingness to travel to client sites, sometimes on short notice, and work in diverse environments. Communication Skills : Strong verbal and written communication skills with the ability to interact effectively with clients and team members. #J-18808-Ljbffr
