A global leader in digital transformation is seeking talented individuals to join their team in Cork, Ireland. This role focuses on managing incident response, backup monitoring, and disaster recovery in a Pharma/Biotech environment. Candidates must have a minimum of 5 years’ experience, strong knowledge of 21 CFR Part 11, and the ability to write SOPs and validation deliverables. Strong organizational and communication skills are essential. Join a team dedicated to improving operational efficiencies and compliance. #J-18808-Ljbffr
A leading technology firm in Cork is seeking a Senior Automation Engineer to oversee pharmaceutical projects involving Delta V. Candidates should possess a degree in automation engineering and have over 3 years of related experience. Responsibilities include generating specifications, leading engineering teams, and managing client interactions. This role offers benefits such as a pension fund, healthcare, and an annual bonus. #J-18808-Ljbffr
A global technology services provider in Dublin is seeking a Computer Systems Validation Engineer to join their managed service team. The role involves validation of computer systems within the pharmaceutical industry, requiring 4-6 years of experience and a Level 7 education. Familiarity with DeltaV and Honeywell systems is advantageous. Ideal candidates should exhibit strong attention to detail and capability to work both under supervision and independently. This position demands a minimum of three days on-site work per week. #J-18808-Ljbffr
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. We’re 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 a Senior Automation Engineer to join 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 #J-18808-Ljbffr
Computer Systems Validation Engineer required as part of the on‑site managed service team The Engineer will work as part of the Cognizant team with our leading pharmaceutical client based in Dublin. Job Responsibilities 4-6 years’ experience in validation with 2-3 years of this in validation of computer systems. Ideal candidate will have automation CSV experience. Exposure to validation in pharma or MedTech essential Attention to detail. Should be able to follow SOPs and WI. Patience with working with multiple documentation at the same time for compare and review. Able to work under supervision initially and able to pick up and work independently after a reasonable period. Support automation system validation team (and wider automation team) on periodic review and improvement projects as requested. Knowledge of automation systems and computer system regulatory requirements will be a plus. Test specification pre-approval, review, and post approval prior to progression to IOQ Change Control Impact Assessments Maintenance, Review and Approval of site Quality documentation e.g. SLIA, CLIA, System Descriptions, CSV Inventory List Yearly commitments made to develop and complete continuous improvements as part of the validation team Co-ordination of changes to ensure timely delivery The Ideal Candidate Level 7 education as a minimum. Computer systems / electronics / engineering degree preferred. Min 3 days per week on site Familiarity with systems such as DeltaV, Honeywell, PLCs (Siemens) and Werum PAS-X Skills CSV GMP PHARMA AUTOMATION PLC DCS #J-18808-Ljbffr
A leading digital transformation firm is seeking a Senior Automation Engineer to join their team in Cork, Ireland. In this role, you will be involved in commissioning and providing on-site support for projects related to Biotech and Pharma clients. The successful candidate will leverage their expertise in automation engineering and project management to lead teams and ensure the successful implementation of solutions. Candidates require a degree and at least 3 years of experience in pharmaceutical manufacturing. #J-18808-Ljbffr
About the Company: 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, Smart Lab, 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 CSV GAMP5 DATA INTEGRITY IT APPLICATIONS PRODUCT LIFE CYCLE #J-18808-Ljbffr
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. We’re 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 a Senior Automation Engineer to join 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 #J-18808-Ljbffr
