Intermediate Automation CSV Engineer

Cognizant; Dublin; On-site; EUR 40,000 - 60,000; Full time

Job summary

A leading digital transformation company in Dublin is seeking a Junior CSV Engineer. You'll utilize your expertise in Automation, focusing on DeltaV, with strong experience in GMP environments. Ideal candidates will have a background in Computer Science or Engineering, with excellent communication skills in English. This role offers a unique opportunity to work with top biotech and pharmaceutical clients.

Qualifications

• Strong proficiency in Automation with DeltaV, with minimum 4 years experience.
• 1-3 years of experience in Computer systems validation.
• 5+ years of experience in a GMP environment.
• Excellent oral and written communication skills in English.

Skills

Automation (DeltaV)

Computer systems validation

GMP environment experience

Data Integrity

Excellent communication skills

Education

BS in Computer Science or Engineering

Tools

MES Delta V

Rockwell

GE

Emerson

ABB

Werum

Siemens

Honeywell

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 compliance.

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 English