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Intermediate Automation CSV Engineer

  • ... Posted on: Feb 06, 2026
  • ... Cognizant
  • ... Dublin, Pennsylvania
  • ... Salary: Not Available
  • ... Full-time

Intermediate Automation CSV Engineer   

Job Title :

Intermediate Automation CSV Engineer

Job Type :

Full-time

Job Location :

Dublin Pennsylvania United States

Remote :

No

Jobcon Logo Job Description :

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 compliCognizant 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.We are looking to add an experienced Junior CSV Engineer to the team of our pharmaceutical client based in Dublin.Requirements: Strong proficiency and experience with Automation, preferably DeltaV for a minimum of 4 years 1-3 years experience with Computer systems validation 5 years experience working in a GMP environment BS in a Computer Science or Engineering field or equivalent experience 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 EnglishCOG2025 #IJP

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Jobcon Logo Position Details

Posted:

Feb 06, 2026

Reference Number:

20748_00064987411

Employment:

Full-time

Salary:

Not Available

City:

Dublin

Job Origin:

APPCAST_CPA

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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 compliCognizant 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.We are looking to add an experienced Junior CSV Engineer to the team of our pharmaceutical client based in Dublin.Requirements: Strong proficiency and experience with Automation, preferably DeltaV for a minimum of 4 years 1-3 years experience with Computer systems validation 5 years experience working in a GMP environment BS in a Computer Science or Engineering field or equivalent experience 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 EnglishCOG2025 #IJP

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