PACIV, a global leader in industrial automation solutions with offices in Ireland, the United States, and Puerto Rico, serving the Life Science, F&B, and Utilities industries, is looking for a Projects Automation Engineer. This is a site-based role. Job Description This role is a Projects Automation Engineer working within a multinational life science manufacturing environment in Dublin, Ireland. Responsible for Automation and IT Systems delivery as part of ongoing LifeCycle Management process. This candidate will be required to work closely with the AIT and LifeCycle Management teams responsible for the full Automation and IT scope and with vendors/partners with responsibility for delivery of systems. Responsibilities of the Role As the Automation Engineer for the Project Team, you will work with other Automation resources, Automation vendors, and partners to deliver automation systems on time and within budget. Develop and/or review Software Development LifeCycle deliverables, compliant with Company standards, including but not limited to: Requirements Specifications Requirements Traceability Matrix Functional Specification Design Specification Code Review Test specification/test script Etc. Work closely with vendors of Automation equipment to ensure deliverables meet project requirements, including the interfacing of new Automation equipment with existing site systems, incl. MES and PI Historian. Work closely with the QA-IT and Computer Systems Validation functions and ensure their requirements are met in all deliverables. Participate in Hardware and Software FATs and SATs to ensure MSD requirements and standards are met. Follow project schedules and document trackers to assist in the management and control of project deliverables. Participate in Automation meetings and support relevant program meetings. Liaise with stakeholders on the overall project to ensure clear communication between all parties. Ensure Automation compliance with Global Policies, Procedures and Guidelines, regulatory requirements and execute current good manufacturing Practices (cGMP) in the performance of day-to-day activities and all applicable job functions. Comply with Global Policies, Procedures and Guidelines, regulatory requirements and execute current Good manufacturing Practices (cGMP) in the performance of day-to-day activities and all applicable job functions. Work collaboratively to drive a safe and compliant culture. Requirements Core Competencies (Technical): Strong experience in the following systems: Siemens and Rockwell PLC, SCADA, and HMIs. Knowledge of and experience with the following systems would be advantageous; Siemens Desigo BAS, Siemens PM server, OSISoft PI, RT Reports, FTView, FactoryTalk. Some knowledge of Computer System Development Lifecycle is preferred. Proficiency in Microsoft Office and job-related computer applications required. Prior experience in a similar role in the Pharmaceutical industry is desirable. Candidates must have a valid EU Work Permit and Irish Residency. Core Competencies (Business): Effective communication and interpersonal skills to interface effectively with all levels of colleagues in a team environment. Self-motivated. Effective time management and multi-tasking skills. Problem-solving skills. Qualifications: Degree Qualification ideally in a related Automation, Engineering, Computer, or other Technical discipline. Compensation Regular staff position, competitive salary, and employee benefits package. Job type: full-time. Job location: site-based role in Dublin, Ireland. #J-18808-Ljbffr
PACIV, a global leader in industrial automation solutions with offices in Puerto Rico, United States and Ireland, and servicing the Life Sciences, F&B and Utilities industries, is looking for a number of DeltaV Engineers for its client site in Cork. Job Description: The potential candidates must have a minimum of 3 Years DeltaV Experience. Junior and Senior Engineers considered for the role. Position Responsibilities /Essential Functions Be part of a project team contributing to the completion of a GMP facility based on the DeltaV platform. Support the project on a day-to-day basis for DeltaV System including: Design document generation. Code development and modification. Batch configuration. Lifecycle documentation generation in line with GAMP (FS, DS, SDS and associated test documents). Modifications to control modules. Generation of new and existing equipment modules. Modification to phase modules. New phase modules generation. Attending daily team meetings. Project leadership. Familiarity with biopharma processes. Requirements: Education: Bachelor’s degree in Engineering (preferably Electrical, Automation, Instrumentation or Chemical). Work Experience: At least 3 years Industrial automation Experience. Experience in the life sciences industries is preferred. Desired Hard Skill Sets: Design, programming, implementation and support for control system/automation projects within regulated environment. Comprehensive understanding of Delta V including Batch essential. Knowledge of other control systems e.g. Siemens, Allen Bradley, programmable logic controllers (e.g. Micrologix, Logix 5000) and HMI/SCADA systems (e.g. iFix, RSView, Wonderware, Batch) desired. Knowledge of Alarm Management, Data Historian, OEE desired. Knowledge and experience of computer system life cycle concepts and FDA regulatory requirements, including 21 CFR Part 1 desired. Desired Soft Skills: Excellent analytical and problem-solving skills to be applied in electrical design, programming and troubleshooting of process and packaging systems. Deals well with uncertainty and pressure. Works well with others, within a team and takes accountability. Result driven and self-motivated. Fluent in English. Strong interpersonal and communication skills (verbal and presentation). Organized, with strong computer literacy such as Excel, etc. Other Requirements Location: Cork, Ireland Travel: To clients, suppliers within Ireland Compensation: Regular staff or contract, competitive salary and employee benefits package. Job Type: Permanent or contract #J-18808-Ljbffr
PACIV, a global leader in industrial automation solutions with offices in Ireland, the United States and Puerto Rico, and serving the Life Science, F&B and Utilities industries, is looking for an experienced Digital Manufacturing Digital Enablement Lead. This is a site-based role with the expectation to be on-site 2-3 days per week. There may be occasions where additional on-site presence is required, depending on project needs. Role Description Reporting to the Digital Manufacturing Project Lead, specifically responsible for the scoping and delivery of the digital elements on the project. This candidate will be required to work closely with the Digital Manufacturing Product teams above site and translate the delivery to scope elements for delivery on project to budget and schedule. Also need to work with the local site stakeholders to identify the capabilities need for a futuristic digital facility whilst defining a clear scope for delivery. The ideal candidate must have a strong understanding of tech transfer processes and the commercialization aspects specific to API site. Role Functions Functions include, but are not limited to, the following: Lead efforts on capital project to deliver digital initiatives. Digital Enablement Strategy for Project which has below and aligns to the site roadmap: Key role to match the capabilities with the above site product line technologies. Liase with multiple operational and digital stakeholders at site to identify and scope. Ensure the capabilities are to the fore first before any discussion on technologies. Liaise with above-site product teams leading global effort to deliver: High level summary of the capabilities and requirements during FEL Stages of projects. Technical understanding of shop floor applications (DeltaV, AVEVA PI, Werum Pax-X MES). Coordinate efforts between above site teams and local site teams to deliver. Good communication skills to explain the operation of digital tools and benefits delivered from. Team player working extensively with wider Digital Manufacturing Team on integrations. Role Requirements BS Degree in Engineering, Computer Science or other technical degree. Strong Knowledge in Digital Deliverables in Automation, IT, AVEVA PI, MES, BAS and related Computer System Validation Efforts. Must have a valid EU work Permit and Irish Residency. Desired: Experience in Delivery of Digital Manufacturing Project Schedule at GMP Site. Experience in roll out of capabilities and collaboration with above site teams to match capabilities to technologies. #J-18808-Ljbffr
Senior MES (Syncade) PACIV Ireland 5+yrs Experience PACIV, a global leader in industrial automation solutions with offices in Ireland, the US, and Puerto Rico, serving the Life Sciences, F&B, and Utilities industries, is looking for a regular employment-based Senior MES Engineer for its customer site in Munster and Leinster area, Ireland. Job Description: Work with the business in gathering and understanding their requirements and translate them into an appropriate solution within the MES system. Work as part of a team in designing and developing electronic batch records/work instructions within the MES solution. Design, develop, and deliver changes to existing/live Recipes. Support, troubleshoot, and resolve issues within the MES system. Participate in design reviews to ensure traceability of requirements. Provide support in troubleshooting and resolving any issues with live Recipes within the MES solution. Work with system vendor to support the root cause and resolution of system issues. Using an object-oriented approach to develop objects that can be shared and used across multiple batch records within the MES solution. Coordinate & participate in solution testing and ensure good testing practices are followed. Possesses general awareness and knowledge of regulatory and quality requirements. Partner with IT peers across manufacturing and solution services to identify solutions to meet business partners’ needs. Required Skills: Knowledge of the Emerson Syncade MES Application is preferable. Experience in Object-Oriented programming languages and demonstrated experience in Visual Basic scripting. Knowledge of XML, XSL, XML, SQL, and Web Services preferable. Demonstrated experience in implementing technical/MES solutions in a GMP environment. Experience in troubleshooting and supporting an MES system or similar system. Ability to work in a development team and take the lead in resolving issues or developing solutions where needed. Experience with direct customer interactions for requirements gathering and translating into a programming solution. Good working knowledge of interfacing ERP systems with MES (preferably SAP). Good working knowledge of interfacing DCS systems with MES (preferably DeltaV). Good working knowledge of interfacing with 3rd party databases such as Historians, Lab Information systems, etc. Knowledge of GMPs, regulatory requirements, and computer system validation. Very good written and verbal communication skills for both technical and non-technical audiences. QUALIFICATIONS & EXPERIENCE ESSENTIAL: Third Level Qualification in Automation, IT Systems, Electronic/Mechatronic Engineering or Equivalent. Minimum 5+ Years’ Experience in Syncade MES. Significant experience of working in a pharmaceutical manufacturing environment (API and OSD). #J-18808-Ljbffr
Position: DeltaV System Administration Engineer. Location: Cork, Ireland. PACIV, a global leader in industrial automation solutions with offices in Ireland, the United States, and Puerto Rico, serving the Life Science, F&B, and Utilities industries, is looking for an experienced DeltaV System Administration Engineer. This is a site-based role. Job Overview This role is a DeltaV System Administration Engineer working within a multinational life science manufacturing environment in Cork, Ireland. The DeltaV System Administrator will work within the automation department to provide automation platform support and perform system administration and maintenance activities on the DeltaV systems at the site. The System Administrator will be required to work with a variety of functions across the site, including operations, project engineering, QA, and IT. As the site operates on a 24/7 basis, the job may involve contact out of hours to provide technical assistance, possible non-scheduled call-in time to respond to plant emergencies, and occasional scheduled call-in time to provide technical cover during technical transfers and major project activity (e.g. commissioning). Responsibilities of the Role Provide day-to-day support and administration for the site DeltaV Systems. Assist in maintaining the DeltaV Systems, including servers, operating systems, security tools, and applications. Engineering scope, design, and support for automation hardware and software upgrade projects, and the implementation of new technologies. Monitor systems health and respond to hardware issues as they arise. Help configure and test platform equipment (e.g. servers, switches, workstations, thin clients) as needed. Co-ordinate and support the upgrade of infrastructure equipment. Interact with other teams to assist in troubleshooting, identify root cause, and provide technical support when needed. Identify and implement solutions to automate manual tasks, where opportunities arise. Co-ordinate system changes and update technical documentation. Requirements Degree in Applied Physics and Instrumentation, Computer Science, Electrical or Electronic Engineering or qualifications in other relevant discipline with appropriate experience. Minimum 5 years’ experience in automation, preferably in the Pharmaceutical Industry. Demonstrated ability to participate in and facilitate decision-making. Demonstrated initiative, good planning and organisational skills, ability to prioritise tasks, commitment to task completion and timelines. Possess a keen technical curiosity and has demonstrated strong problem-solving skills and a desire for continuous improvement. Strong collaborative skills with an ability to work effectively in a team environment. Demonstrated ability to influence peers and business partners. Demonstrated strong written and verbal communications skills. Self motivated, ability to work independently. Knowledge of GMP, regulatory requirements, computer system validation. Proficient in English. Must have Valid EU Work Permit and Irish Residency. PLEASE NO AGENCIES. Preferable: DeltaV training. Experience with industrial networks/protocols, for example: OPC, Ethernet IP. Experience with virtualisation technologies, thin clients. Professional certifications. Experience with Kneat electronic testing. #J-18808-Ljbffr
DeltaV Engineer - 5 to 10 Years Experience PACIV, a global leader in industrial automation solutions with offices in Puerto Rico, the United States, and Ireland, and servicing the Life Sciences, F&B, and Utilities industries, is looking for Experienced DeltaV Engineers for its office in Ireland. Job Description: The potential candidates must have 5-10 years of DeltaV experience, including Batch. Position Responsibilities / Essential Functions: Be part of a project team contributing to the completion of a biopharma project based on the DeltaV platform. Support the project on a day-to-day basis for DeltaV System including: Code development and modification. Batch configuration. Lifecycle documentation generation in line with GAMP (FS, DS, SDS, and associated test documents). Modifications to control modules. Generation of new and existing equipment modules. Modification to phase modules. New phase modules generation. Attending daily team meetings. Project leadership. Familiarity with biopharma processes. Requirements: Education: Bachelor’s degree in Engineering (preferably Electrical, Automation, Instrumentation, or Chemical). Work Experience: From Five (5) to Ten (10) years of industrial automation experience. Experience in the life sciences industries is preferred. Desired Hard Skill Sets: Design, programming, implementation, and support for control system/automation projects within a regulated environment. Comprehensive understanding of DeltaV, including Batch essential. Knowledge of other control systems (e.g., Siemens, Allen Bradley, programmable logic controllers like Micrologix, Logix 5000) and HMI/SCADA systems (e.g., iFix, RSView, Wonderware, Batch) desired. Knowledge of Alarm Management, Data Historian, OEE desired. Knowledge and experience of computer system life cycle concepts and FDA regulatory requirements, including 21 CFR Part 11 desired. Desired Soft Skills: Excellent analytical and problem-solving skills to be applied in electrical design, programming, and troubleshooting of process and packaging systems. Deals well with uncertainty and pressure. Works well with others, within a team, and takes accountability. Result-driven and self-motivated. Strong interpersonal and communication skills (verbal and presentation). Organized, with strong computer literacy such as Excel, etc. Other Requirements: Location: Ireland Must have a valid EU Work Permit and Irish Residency Travel: To clients, suppliers within Ireland Compensation: Regular staff position, competitive salary, and employee benefits package. #J-18808-Ljbffr
