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
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. Experience/Attributes: Proven experience as a Senior 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 Siemens Step or Rockwell ControlLogix Good analytical & problem solving skills Excellent communication skills Leadership abilities, works well in a team environment Responsibilities: Work as part of a team to develop implement and maintain packaging automation systems in the pharmaceutical manufacturing Facility. Develop review and approve new and updated software standards. Provide automation expertise to the engineering and operations department on design and sustaining decisions. Liaise closely with internal stakeholders to successfully support packaging operations. Develop and implement standard operating procedures to ensure the future compliance of all automation systems. Ensure all new software is delivered and maintained in a compliant and qualified state. Provide support for validation activities. Participate in cross-functional teams to drive optimization of processes and equipment. Assist in training personnel on specific automation aspects of equipment. Design and implement solutions across automation platforms in line with the site change control procedures. Develop review and approve design documentation that support New Product Introductions (NPI) Essential Skills: 4+ Years Automation Experience in a GMP environment Automation PLC experience required in Siemens S7, Allen Bradley PLCs Skills: PLC OEM HMI Scada Vb.Net MES PASX
Cognizant Company 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. About the role: We are looking for an OSI PI Engineer to join our OSI team for a site-based project in Cork. The Senior OSIsoft PI Software Engineer needs to have an in-depth experience of OSI Data Historian Systems, Control Systems and Process Analysis. The successful candidate should have an extensive background in Software Engineering with experience in systems analysis and software development within the pharmaceutical industry. He/she should be highly motivated, an innovative thinker and self-starter, with excellent interpersonal and problem-solving skills What you will do: Designing and implementing highly reliable and large-scale systems with HA collectives and federated designs Installing, configuring, validating, and tuning PI Servers and interfaces Implementing analytic solutions with PI Asset Framework Analytics, PI ACE, PI Notifications and Performance Equations Installing and tailoring client software including Coresight, ProcessBook, DataLink, Rtreports and PI WebParts. Working with PLC and DCS-based control systems, building management systems, and/or energy management systems Qualifications: Undergraduate degree in IT, Automation, Science or Engineering, or related discipline, or equivalent work experience Skills: OSIsoftPI Historian trained and certified Solid understanding of the OSI PI system architecture with 4 years plus experience in PI System implementations Excellent knowledge of SCADA, PLC, OPC, Continuous/Batch Historians, MES systems and DCS-based control systems including network topology concepts. Expert understanding of PI Architecture. 24-48 months supporting PI Projects and Systems. Advanced understanding of how SQL Databases are set up & administered with respect to PI systems in addition to Oracle installation query and view structuring. Ability to write instructions for installation configuration and troubleshooting of interfaces in line with TQS standards and OSI recommendations. Can develop and design PI Systems and GxP Documentation without supervision. Good technical knowledge of network security and TCP/IP protocol Good technical knowledge of networks and related hardware and software Drafts Validation document lifecycle including installation/operational qualification and design specification creation and execution across multiple successful projects of varying scope. Provides resourcing estimates and technical configurations of client quotations to the Business Development Team. Mentors train and support System Analysts and Software Consultants. Superb analytical and troubleshooting skills and methodical approaches to solving difficult problems Excellent verbal and written communication skills PI Historian Scada OSIsoftPI Skills: OSI Scada Historian
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: The MES Engineer will be responsible for implementing System\MES recipe changes and managing the day to day issues that arise in the support of Electronic Batch Records, Weigh and Dispense and Equipment Management modules on our Emerson Syncade MES solution. The position will work within a collaborative MES team at a large multi-national Biotech manufacturing facility in Cork and will be required to have excellent communication/interpersonal skills with the ability to work on their own initiative. Experience of working in a pharmaceutical API manufacturing operation is desirable. S/he is expected to be self-motivated and develop an understanding of the business. Requirement Create business process flow diagram for pharmaceutical product recipes based on the paper batch record or source documents. Gather MES Site specific requirement analysis to develop URS and FRS. Logically breakdown the recipes/Mfg. process to configure the recipe in to Syncade Develop/create MBR design elements (building blocks) and workflows in Syncade for repetitive use in MBR creation to expedite the process. Gather master data and configure in Syncade Development/Quality/Production Environment. Integrating Syncade with SAP and other automation systems using standard interface component of MBR design. Lead the recipe design session with business process SMEs. Design MBR/recipe equipment workflow/ status diagram. Responsibilities Development, implementation, and support of MES recipes. The ability to produce high-quality, well documented configuration that is easily maintainable Work with various site teams to configure and support interfaces to other systems that MES interacts with such as ERP, Automation and Lab systems. Investigate and troubleshoot problems which occur and determine solutions or recommendations for changes and/or improvements Implement system design changes in accordance with company Quality Standards and Practices Translate business requirements into design and perform testing of new MES recipes and changes Generate computer system validation documentation in accordance with site procedures and GMP guidelines Recognize the importance of the quality control function in pharmaceutical production, the MES Software Engineer should display a high level of integrity in the performance of his/her work. S/he should be capable of relating well to other people with whom s/he comes in contact, both within and outside of the MES Team The role will evolve to require Out Of Hours Support in the future Skills: MES Syncade troubleshooting recipe designs
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. Experience/Attributes: Junior CSV Engineer - The Computer Systems Validation (CSV) Engineer will develop and execute protocols and test scripts identify gaps and consult on and direct plans for resolution. This person is responsible for writing GxP computer validation and 21 CFR Part 11 related documentation such as assessments plans URS FRS RTM and summary reports. Responsibilities BS in a Computer Science or Engineering field or equivalent experience 1-3 years experience with Computer systems validation 1 years experience working in a GMP environment Experience in Data Integrity with GAMP and 483 compliance consent decree experience deep 21CFR Part 11 experience is a plus Experience in biotech and pharma is preferred over medical device Experience with MES Delta V PI is a plus. We use all major systems as we serve a multitude of clients. Rockwell GE Emerson ABB Werum Siemens Honeywell and their associated platforms PAS-X Syncade FactoryTalk PharmaSuite Control Logix PLM Simatic iFix Wonderware Siemens etc. Excellent oral and written communication skills in English/Fluent in English Skills: Validation 21CFR
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: The MES Support Engineer will be responsible for implementing System\MES recipe changes and managing the day to day issues that arise in the support of Electronic Batch Records, Weigh and Dispense and Equipment Management modules on our Emerson Syncade MES solution. The position will work within a collaborative MES team at a large multi-national Biotech manufacturing facility in Cork and will be required to have excellent communication/interpersonal skills with the ability to work on their own initiative. Experience of working in a pharmaceutical API manufacturing operation is desirable. S/he is expected to be self-motivated and develop an understanding of the business. Responsibilities Maintain the incident queue in Service Now and manage & resolve issues as they arise in a timely manner. Initiate and implement Change Control activities in accordance with Quality Standards and Practices Investigate and troubleshoot problems which occur and determine solutions or recommendations for changes and/or improvements The ability to produce high-quality, well documented configuration that is easily maintainable Prioritize support activities in line with project schedules Perform testing of new MES recipes and changes Generate computer system validation documentation in accordance with site procedures and GMP guidelines Follow all relevant Environmental, Health and Safety procedures and assist in incident investigations as required. Recognise the importance of the quality control function in pharmaceutical production, the MES Support Engineer should display a high level of integrity in the performance of his/her work. S/he should be capable of relating well to other people with whom s/he comes in contact, both within and outside of the MES Team The role will evolve to require Out Of Hours Support in the future Requirements Minimum 3-5 years experience supporting IT applications e.g. troubleshooting, managing incidents and change controls, design documentation, test case development, system & integration testing Experience implementing changes for IT applications in a GMP environment would be an advantage MES Recipe Authoring experience, knowledge of the Emerson Syncade MES solution would be an advantage but not required. Knowledge of programming and Visual Basic with experience in configuration management and deployment of developed code. MS SQL server experience would be an advantage Past proven experience engaging business users to ensure that appropriate business needs are clearly 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. The successful candidate must be a highly motivated individual who is delivery focused and has experience of working successfully across multiple business & functional teams. Skills: MES Syncade troubleshooting recipe designs
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 looking for dedicated, innovative and driven talent to join our expanding team in Dublin. We're currently looking for a full-time MES Engineer, and the role comes with a generous salary and benefits package. As an MES Engineer, you will be responsible for implementing System/MES recipe changes and managing the day-to-day issues that arise in the support of Electronic Batch Records, Weigh and Dispense and Equipment Management modules on ourEmerson Syncade MES solution. In your first few weeks in this role, you can expect to: Maintain the incident queue in Service Now and manage and resolve issues as they arise in a timely manner Initiate and implement change control activities in accordance with quality standards and practices Investigate and troubleshoot problems which occur and determine solutions or recommendations for changes and/or improvements Prioritise support activities in line with project schedules. To apply for this MES Engineer role, you will need a minimum of 3 years of experience supporting IT applications, e.g. troubleshooting, managing incidents and change controls, design documentation, test case development, system and integration testing. You will also require the following: Create business process flow diagram for pharmaceutical product recipes based on the paper batch record or source documents. Gather MES Site specific requirement analysis to develop URS and FRS. Logically breakdown the recipes Mfg. process to configure the recipe in to Werum PAS-X Develop/create MBR design elements (building blocks) and workflows in Werum PAS-X for repetitive use in MBR creation to expedite the process. Gather master data and configure in Werum PAS-X Development/Quality/Production Environment. Integrating Werum PAS- X with SAP and other automation systems using standard interface component of MBR design. Lead the recipe design session with business process SMEs. Design MBR/recipe equipment workflow/ status diagram based on the Business process flow. Create solution design and configuration document. Prepare key user training documents and impart key user training. Provide assistance in business SOP creation. A Bachelors degree in Computer Science Computer Engineering Computer Information Systems or a related field (Technology Management Chemical Engineering) Intermediate level Werum PAS-X experience desired Werum PAS-X product hands-on experience for Full application configurations including interface with SAP and automation systems. In-depth of knowledge of Bio Pharma processes Creation of business process flow diagram Master Batch Record creation in Werum PAS-X Knowledge on Industry Standards S88 and ISA S95 Pharmaceutical validation concept cGMP and GDP standards and GAMP Standards Good verbal written communication 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. Please reach out to our friendly and welcoming team today to apply for this full-time hybrid MES Support Engineer position in Dublin. . 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. Skills: MES Syncade PAS-X MBR URS FRS Batch Record
Cognizant are looking for an OSI PI Engineer to join our OSI team in Dublin. The OSIsoft PI Software Engineer needs to have an in-depth experience of OSI Data Historian Systems, Control Systems and Process Analysis. The successful candidate should have an extensive background in Software Engineering with experience in systems analysis and software development within the pharmaceutical industry. They should be highly motivated, an innovative thinker and self-starter, with excellent interpersonal and problem-solving skills What you will do: Designing and implementing highly reliable and large-scale systems with HA collectives and federated designs Installing, configuring, validating, and tuning PI Server and interfaces Implementing analytic solutions with PI Asset Framework Analytics, PI ACE, PI Notifications and Performance Equations Installing and tailoring client software including Coresight, ProcessBook, DataLink, Rtreports and PI WebParts. Working with PLC and DCS-based control systems, building management systems, and/or energy management systems Qualifications: Undergraduate degree in IT, Automation, Science or Engineering, or related discipline, or equivalent work experience Skills: OSIsoft PI Historian trained and certified Solid understanding of the OSI PI system architecture with 4 years plus experience in PI System implementations Excellent knowledge of SCADA, PLC ,OPC, Continuous/Batch Historians, MES systems and DCS Based control systems including network topology concepts. Expert understanding of PI Architecture. 24-48 months supporting PI Projects and Systems. Advanced understanding of how SQL Databases are setup & administered with respect to PI systems in addition to Oracle installation query and view structuring. Ability to write instructions for installation configuration and troubleshooting of interfaces in line with TQS standard and OSI recommendations. Can develop and design PI Systems and GxP Documentation without supervision. Good technical knowledge of network security and TCP/IP protocol Good technical knowledge of networks and related hardware and software Drafts Validation document lifecycle including installation/operational qualification and design specification creation and execution across multiple successful projects of varying scope. Provides resourcing estimates and technical configurations of client quotations to the Business Development Team. Mentors trains and supports System Analysts and Software Consultants. Superb analytical and troubleshooting skills and methodical approaches to solving difficult problems Excellent verbal and written communication skills Skills: PI Historian Scada OSIsoftPI
