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Cognizant Technology Solutions Ireland
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  • Cognizant is a world leader in delivering digital transformation solutions to Life Sciences. Through our knowledge and expertise in Automation, MES & Digital, we deliver stable manufacturing systems that are optimized to improve operational efficiencies, whilst maintaining compliance. Our specialist engineering teams have the aptitude to deliver and support Pharma 4.0 architectures and solutions covering all IT, OT and IoT applications, infrastructures and services. Operating across 5 continents and with over 300.000 skilled employees, Cognizant partners with the leading Life Sciences companies globally to provide performance improvements, reduced costs and improve time to market. We are your single end to end partner for consultancy, design implementation, optimization and support for all applications in the Pharmaceutical and Biotechnology Manufacturing stack. We're looking for dedicated, innovative and driven talent to join our expanding team. Requirement: Core functions of the role include Incident Response, Backup Monitoring, Disaster Recovery, Account/Group Management, Supporting Service Providers, Patch Deployment. Experience with Service Now, Trackwise, Veeva Quality Docs, ALM, SmartLab, Empower an advantage. Essential Skills: Minimum 5 years experience in a Pharma/Biotech environment. Strong knowledge of 21 CFR Part 11, EU GMP Annex 11 principles. Ability to write and execute Change Controls, Work Items and CAPAs. Experience implementing changes for IT applications in a GMP environment. Ability to write SOPs and other validation deliverables such as Design Specifications, System Overviews and Security Plans. Experience leading and writing deviation investigations. Strong oral and written communication skills. Self-motivated, detail-oriented and excellent organizational and time management skills Skills: GMP pharma ServiceNow 21CFR Trackwise

  • Cognizant is a world leader in delivering digital transformation solutions to Life Sciences. Through our knowledge and expertise in Automation, MES & Digital, we deliver stable manufacturing systems that are optimized to improve operational efficiencies, whilst maintaining compliance. Our specialist engineering teams have the aptitude to deliver and support Pharma 4.0 architectures and solutions covering all IT, OT and IoT applications, infrastructures, and services. Operating across 5 continents and with over 300.000 skilled employees, Cognizant partners with the leading Life Sciences companies globally to provide performance improvements, reduced costs and improve time to market. We are your single end to end partner for consultancy, design implementation, optimization, and support for all applications in the Pharmaceutical and Biotechnology Manufacturing stack. Were looking for dedicated, innovative, and driven talent to join our expanding team. The successful candidates would be required to have a minimum of 5 to 8 years of Emerson DeltaV DCS batch or operation experience. These long-term roles offer an excellent opportunity to grow within Zenith Technologies. Good knowledge of GAMP lifecycle and quality management processes employed in the pharmaceutical and biotechnology sectors Experience implementing Emerson DeltaV automation solutions for clients in the Pharmaceutical and/or Biotechnology industries Preferably with experience with design, development, coding, and testing of DeltaV DCS. Preparation of functional specification and design specification documentation, and testing of automation systems Understanding of S88 / Batch Proficiency & Biotech Conversant an advantage. Understanding on all Project Lifecycle phases and tasks Configuration and programming experience, CMs, EMs, Unit Classes, Recipes, Controllers and Graphics Knowledge of virtualization is added advantage Experience in supporting client/sites for NC, CAPA, Root cause analysis and automation Change control management Good analytical & problem-solving skills Excellent communication skills Must work well in a team environment Self-starter who can get the job done despite obstacles Requires a bachelors degree or foreign equivalent in Chemical, Electrical or Bio-Process Engineering, or related field Skills: DeltaV Allen Bradley Automation PLC Scada HMI ABB

  • Honeywell Automation Engineer Cognizant is a world leader in delivering digital transformation solutions to Life Sciences. Through our knowledge and expertise in Automation, MES & Digital, we deliver stable manufacturing systems that are optimized to improve operational efficiencies, whilst maintaining compliance. Our specialist engineering teams have the aptitude to deliver and support Pharma 4.0 architectures and solutions covering all IT, OT and IoT applications, infrastructures, and services. Operating across 5 continents and with over 300.000 skilled employees, Cognizant partners with the leading Life Sciences companies globally to provide performance improvements, reduced costs and improve time to market. We are your single end to end partner for consultancy, design implementation, optimization, and support for all applications in the Pharmaceutical and Biotechnology Manufacturing stack. Were looking for dedicated, innovative, and driven talent to join our expanding team. The successful candidate will manage and provide for the development of all DCS, PLCs and SCADA systems to industry standards, GAMP5. Successful candidate will provide and ensure the design, development, maintenance and troubleshooting of automated systems on site, is completed in a compliant manner as per GAMP5 and EU GMP Annex 11. Desired Background/Experience/Attributes: Proven experience as An Automation Engineer with increased levels of responsibility Experience designing, implementing, and supporting automation solutions for clients in the Pharmaceutical and/or Biotechnology industries. Good knowledge of GAMP lifecycle and quality management processes employed in the pharmaceutical sector. Experience with Honeywell BMS Good analytical & problem-solving skills Excellent communication skills Leadership abilities, works well in a team environment. Responsibilities: Day to day automation incident triage & resolution User Access Requests Batch Record Comment Requests Automation Preventative Maintenance Periodic Reviews for automation Training Automation systems as required. CAPA Automation child actions IRs Automation Cross Functional collaboration Knowledge Base for Automation systems Essential Skills: 3+ Year Automation Experience in a GMP environment Automation PLC experience required Honeywell, Requires a bachelors degree or foreign equivalent in Chemical, Electrical or Bio-Process Engineering, or related field Skills: honeywell gmp automation gxp pharma plc batch

  • Role Overview: The Managed Service Lead is responsible for overseeing the delivery, performance, and continuous improvement of technology managed services supporting laboratory systems and MES platforms within a regulated pharmaceutical environment. This role ensures compliance with GxP requirements, drives operational excellence, and acts as the primary point of contact between the service provider, internal stakeholders, and external vendors. Required Skills & Experience: Strong experience in technology/software service management (ITSM) within the pharmaceutical or life sciences sector. Background in life sciences software project management desirable Familiarity with GxP regulations and their application to Life Sciences manufacturing, Labs and MES environments. Experience of performance management of direct reports in site-based teams essential Proven track record managing complex, multi-vendor service landscapes. Excellent communication, stakeholder management, and problem-solving skills. Technical background in Software Development, Process Automation or Engineering, Computer Systems Validation desirable Familiarity with laboratory informatics (e.g., LIMS, ELN) and MES platforms. Strong customer-focussed communication skills ITIL certification or equivalent is a plus. Key Responsibilities: Service Delivery Management: Oversee day-to-day operations of managed services for Labs and MES, ensuring adherence to SLAs, KPIs, and regulatory standards. GxP Compliance: Ensure all services and changes are delivered in accordance with GxP, data integrity, and audit requirements. Maintain documentation and support regulatory inspections. Stakeholder Engagement: Act as the main liaison between business users, IT, quality, and third-party vendors. Manage escalations and ensure effective communication. Incident & Problem Management: Lead the resolution of incidents, problems, and service requests. Drive root cause analysis and implement corrective/preventive actions. Continuous Improvement: Identify opportunities to optimize service delivery, enhance system reliability, and reduce operational risk. Change & Release Management: Oversee changes to Lab and MES systems, ensuring proper validation, testing, and documentation in line with GxP. Team Leadership: Lead and mentor a team of software service delivery professionals and technical specialists Skills: csv automation mes it ot people management team lead

  • Automation & OT Service Lead Role Overview: The Automation and OT Managed Service Lead is responsible for overseeing the delivery of projects and support services across automation and OT systems within a regulated pharmaceutical environment. This role requires acting as the primary point of contact for our team on our client site including management of overall team resourcing, performance and development. This role is 3 days per week on site. Required Skills & Experience: Excellent people management skills across multiple disciplines. Strategic Thinker, to drive innovative thinking and add value to the service provided. Strong communication skills for engagement with client and internal stakeholders as well as team members Excellent presentation and facilitation skills Ability to lead, motivate and engage the team to continually deliver Technical background in Process Automation and/or OT systems essential Background in life science project management desirable Key Responsibilities: Overall accountability for all Cognizant activities on the client site. Responsible for onsite project delivery, working with the site project manager to resource, budget and deliver all onsite projects on time. Responsible for onsite managed service team to resource and deliver system support, system change and innovation to our client. Support our team with development and career progression. Resourcing for Project and Manage Service requirements to meet client needs. Measure and report team performance to Cognizant and client stakeholders against formal KPIs. Manage our service budget and ensure control of Capex spend for client projects. Act as primary POC for all client requirements related to Automation and OT systems. Working closely with Cognizant Delivery Leaders and our Sales team, to manage and develop our Site Services offering. Skills: gmp people mangagment Automation ITOT

  • Cognizant is a world leader in delivering digital transformation solutions to Life Sciences. Through our knowledge and expertise in Automation, MES & Digital, we deliver stable manufacturing systems that are optimized to improve operational efficiencies, whilst maintaining compliance. Our specialist engineering teams have the aptitude to deliver and support Pharma 4.0 architectures and solutions covering all IT, OT and IoT applications, infrastructures and services. Operating across 5 continents and with over 300.000 skilled employees, Cognizant partners with the leading Life Sciences companies globally to provide performance improvements, reduced costs and improve time to market. We are your single end to end partner for consultancy, design implementation, optimization and support for all applications in the Pharmaceutical and Biotechnology Manufacturing stack. We're looking for dedicated, innovative and driven talent to join our expanding team. About the Role: TheLab Systems Engineer will work with a team onsite with our client in Dublin and be responsible for the validation of PC Controlled Analytical Laboratory Systems for their facility. The candidate will need to have experience in validation and support of Laboratory systems/IT applications. The candidate is expected to be self-motivated and develop an understanding of the business. Experience of working in a pharmaceutical API manufacturing operation is desirable. Responsibilities Execute and Monitor data backups and resolve issues as they arise in a timely manner. Request Security patching updates from Global Team, manage the deployment and resolve issues in a timely manner. Build PCs and connect them to network Install and configure security tools on PCs Perform Disaster recovery testing Account creation and password resets Administration of vendor accounts Perform Security Reviews for Computerized Instruments following up on gaps or discrepancies. Execute test scripts, analyze test results and determine the acceptability of results against pre-determined criteria. Investigate and troubleshoot problems which occur and determine solutions or recommendations for changes and/or improvements. Work directly with Lab Validation Engineers, System Administrators/Subject Matter Experts and Quality Assurance Representatives ensuring ongoing compliance with Lilly Quality Standards and Practices Follow all relevant Environmental, Health and Safety procedures and assist in incident investigations as required. Recognize the importance of the quality control function in pharmaceutical production, the IT Support Engineer should display a high level of integrity in the performance of his/her work. Requirements Suitability degree qualified IT/ Automation/ or equivalent engineer Minimum 2-4 years experience supporting Lab systems/IT applications e.g. requirements gathering, design documentation, test case development, system & integration testing Minimum 2 years experience in a regulated environment Experience working in a Win 7 environment is an advantage Past proven experience engaging business users to ensure that appropriate business needs are clearly defined, communicated and delivered at or above expectations Strong oral and written communication skills are required, with proven ability to communicate and build relationships cross-functionally Experience of ER/ES and 21 CFR part 11 compliant software desirable Experience of use of Validation tools, Security tools and Diasaster recovery applications Skills: LIMS Empower

  • Do you have Automation Engineer and Pharmaceutical Manufacturing experience, and are you seeking a new job? Cognizant is looking for a Senior Automation Engineer (DeltaV) in Dublin, and the remote role comes with an attractive salary and benefits package. You'll be working with a collaborative and inclusive company and will be involved in commissioning and on-site support activities. As a Senior Automation Engineer, you will join a project team in Dublin where you will be involved in commissioning and on-site support activities. You will also generate functional specifications, design and test specifications for recipes, phase sequences, equipment modules, control modules, customized logic and HMI Graphics based on customer User Requirement Specifications (URS). In your first few weeks in this Senior Automation Engineer role, you can expect to: Configuration and Testing of Recipes, Phases, equipment modules, Control Logic and Interlock Schemes based on design and test specifications Lead teams of Engineers and manage the project resources, scheduling task assignments, client interaction, coordination amongst different vendors and remote engineering office teams Batch Process upgrading on the DeltaV platform for Pharmaceutical clients. To apply for this DeltaV Automation Engineer role, you will need to be a degree-qualified automation engineer with over six years of pharmaceutical manufacturing experience. You will also require the following: S88 / Batch Delta V expert Expert understanding of all project lifecycle phases and tasks Demonstrable project management skills Track record demonstrating ability to lead a complete project Ability to work independently. You'll receive an excellent salary and benefits package for your knowledge, expertise and flexibility. At Cognizant, taking care of employees is a priority: You can pursue innovative career tracks and opportunities here You can enhance your professional development through education and dedicated training Well give you the skills you need to keep pace with the changing workplace while our compensation, benefits and wellness packages help you stay healthy and plan for the future. To apply for this inclusive and collaborative remote full-time Delta V Engineer job, don't hesitate to contact Cognizant today. At Cognizant, we engineer modern businesses to improve everyday life because we're dedicated to making a lasting impact. Cognizant (Nasdaq: CTSH) engineers modern businesses. We help our clients modernize technology, reimagine processes and transform experiences so they can stay ahead in our fast-changing world. Together, we're improving everyday life. Skills: Delta V Plc Programming Scada DCS Allen Bradley Siemens PLC Benefits: Group Life Assurance Dental Insurance Paid Holidays Performance Bonus Work Laptop

  • Cognizant is a world leader in delivering digital transformation solutions to Life Sciences. Through our knowledge and expertise in Automation, MES & Digital, we deliver stable manufacturing systems that are optimised to improve operational efficiencies, whilst maintaining compliance. Our specialist engineering teams have the aptitude to deliver and support Pharma 4.0 architectures and solutions covering all IT, OT and IoT applications, infrastructures and services. Operating across 5 continents and with over 850 skilled employees, Cognizant partners with the leading Life Sciences companies globally to provide performance improvements, reduced costs and improve time to market. We are your single end to end partner for consultancy, design implementation, optimisation and support for all applications in the Pharmaceutical and Biotechnology Manufacturing stack. Were looking for dedicated, innovative and driven talent to join our expanding team. About the Role: Cognizant (LSMG) are currently executing a number of projects for large Biotech and Pharma clients in Ireland.We are looking for dedicated, innovative and driven talent to join our expanding teams. We require aSenior Automation Engineertojoin a project team in Cork where you will be involved in commissioning and on-site support activities. Responsibilities Generation of Functional specification, Design and Test Specifications for Recipes, Phase Sequences, Equipment Modules, Control Modules, customized logic and HMI Graphics based on customer User Requirement Specification (URS). Configuration and Testing of Recipes, Phases, Equipment Modules, Control Logic and Interlock Scheme based on Design and Test Specifications. Lead teams of Engineers and manage the Project Resources, Scheduling Task assignments, Client interaction, co-ordination amongst different vendors, co-ordination between front office team and remote engineering office teams. Batch Process upgrading on DeltaV platform for Pharmaceutical clients. Interact with customer for Reviewing Design Specifications and Test Specifications. Lead teams for Installation Qualification and operational Qualification (SAT) at client site. Involvement for Site Commissioning activities. Requirements Suitability degree-qualified automation engineer with over 3 years pharmaceutical manufacturing experience. S88 / Batch Delta V expert. Expert understanding on all Project Lifecycle phases and tasks. Demonstrable Project Management Skills (Scope, Cost, Schedule Management). Ability to liaise directly with client on design issues. Track record demonstrating an ability to lead a complete project. Ability to work independently. Proficient in spoken and written English. Thorough understanding of system (installing, rebuilding etc.). Skills: Delta V Plc Programming dcs Automation PLC Scada PHARMA Benefits: shift flex Pension Fund healthcare Annual Bonus / 13th Cheque

  • Cognizant is a world leader in delivering digital transformation solutions to Life Sciences. Through our knowledge and expertise in Automation, MES & Digital, we deliver stable manufacturing systems that are optimised to improve operational efficiencies, whilst maintaining compliance. Our specialist engineering teams have the aptitude to deliver and support Pharma 4.0 architectures and solutions covering all IT, OT and IoT applications, infrastructures and services. Operating across 5 continents and with over 850 skilled employees, Cognizant partners with the leading Life Sciences companies globally to provide performance improvements, reduced costs and improve time to market. We are your single end to end partner for consultancy, design implementation, optimisation and support for all applications in the Pharmaceutical and Biotechnology Manufacturing stack. Were looking for dedicated, innovative and driven talent to join our expanding team. About the Role: Cognizant (LSMG) are currently executing a number of projects for large Biotech and Pharma clients in Ireland.We are looking for dedicated, innovative and driven talent to join our expanding teams. We require aSenior Automation Engineertojoin a project team in Cork where you will be involved in commissioning and on-site support activities. Responsibilities Generation of Functional specification, Design and Test Specifications for Recipes, Phase Sequences, Equipment Modules, Control Modules, customized logic and HMI Graphics based on customer User Requirement Specification (URS). Configuration and Testing of Recipes, Phases, Equipment Modules, Control Logic and Interlock Scheme based on Design and Test Specifications. Lead teams of Engineers and manage the Project Resources, Scheduling Task assignments, Client interaction, co-ordination amongst different vendors, co-ordination between front office team and remote engineering office teams. Batch Process upgrading on DeltaV platform for Pharmaceutical clients. Interact with customer for Reviewing Design Specifications and Test Specifications. Lead teams for Installation Qualification and operational Qualification (SAT) at client site. Involvement for Site Commissioning activities. Requirements Suitability degree-qualified automation engineer with over 3 years pharmaceutical manufacturing experience. S88 / Batch Delta V expert. Expert understanding on all Project Lifecycle phases and tasks. Demonstrable Project Management Skills (Scope, Cost, Schedule Management). Ability to liaise directly with client on design issues. Track record demonstrating an ability to lead a complete project. Ability to work independently. Proficient in spoken and written English. Thorough understanding of system (installing, rebuilding etc.). Skills: Delta V Plc Programming dcs Automation PLC Scada PHARMA

  • Do you have lab equipment validation experience, and are you seeking a new job in Cork? Cognizant is looking for an IT CSV Engineer, and the hybrid role comes with an attractive salary and benefits package, including the chance to join a collaborative team. The IT CSV Engineer will be responsible for the validation of Lab Systems in QCL Labs and Manufacturing Operations. You will provide systems validation and compliance expertise for newly purchased instruments. In your first few weeks in this Validation Engineer role, you can expect to: Manage lab equipment validation projects from software install to business release Priorities CSV activities in line with the project schedule and monitor budgets Generate computer system validation documentation, e.g., Design Spec, Configuration Spec, Testing, Security Plan, Test Summary Report, in accordance with site procedures and GMP guidelines Review software release notes. To apply for this CSV Engineer role, you will need a minimum of 3 years of experience supporting and validating lab equipment, updating documentation, system testing, troubleshooting. You will also require the following: Experience analysing and challenging s/w to identify gaps Knowledge of 21CFR Part 11 requirements, ER/ES and data integrity guidelines Excellent oral and written communication skills, with the proven ability to communicate and build relationships cross-functionally. At Cognizant, taking care of employees is a priority: You can pursue innovative career tracks and opportunities here You can enhance your professional development through education and dedicated training Well give you the skills you need to keep pace with the changing workplace while our compensation, benefits and wellness packages help you stay healthy and plan for the future. To apply for this inclusive and collaborative full-time IT CSV Engineer job, please contact Cognizant today. At Cognizant, we engineer modern businesses to improve everyday life. Because we're dedicated to making a lasting impact. Cognizant (Nasdaq-100: CTSH) is one of the world's leading professional services companies, transforming clients' business, operating and technology models for the digital era. Our unique, industry-based, consultative approach helps clients envision, build, and run more innovative and efficient businesses. Headquartered in the U.S., Cognizant is ranked 185 on the Fortune 500 and is consistently listed among the most admired companies globally. Learn how Cognizant helps clients lead with . Skills: IT CSV gmp GAMP5 data integrity 21CFR PART 11 Design spec

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