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We are looking for an Automation Engineer with DeltaV DCS experience to support MES / EBR validation in a GMP-regulated manufacturing environment. This role ensures system data, batch records, and validation documentation are accurate, traceable, and inspection-ready.
Job Responsibility
Support validation activities for MES / EBR systems in a GMP-regulated manufacturing environment
Review User Requirement Specifications, functional specifications, data mapping documents, test scripts, protocols, validation reports, and other related documentation
Assess data flow between DeltaV DCS and MES / EBR systems to ensure accuracy, completeness, and traceability
Review or prepare validation test scripts to confirm that the system performs as intended
Support the execution, review, and documentation of validation testing
Identify documentation gaps, system issues, or data integrity concerns and support follow-up actions
Ensure validation documentation complies with GMP, GDP, and data integrity expectations
Collaborate closely with Manufacturing, Automation, IT, Quality, and Validation teams
Support audit and inspection readiness by maintaining clear, complete, and compliant validation records.
Requirements
You have experience in pharmaceutical, biotechnology, or another GMP-regulated manufacturing environment
You have hands-on experience with DeltaV DCS
You have experience with MES, EBR, batch records, computerized system validation, or related validation activities
You have an academic background in Engineering, Automation, Life Sciences, IT, or a related discipline
You are fluent in English
You demonstrate strong attention to detail and a strong documentation mindset
You are able to work cross-functionally with Automation, Manufacturing, Quality, Validation, and IT teams.
What we offer
Global Diversity: Be part of an international team of 110+ nationalities
Trust and Growth: 70% of our leaders starting at entry-level
Continuous Learning: Internal Academy and over 250 training modules