Back
Login to See Your Match Score
Create a free account or log in to unlock your CV match score across:
Tier-1 employer but highly specialized automation/DeltaV/PI pharma role reduces applicant density.
Role requires pharma-specific validation and DeltaV/PI historian expertise, limiting cross-industry transferability.
Mandatory 10+ years plus DeltaV, PI, and pharma validation (21 CFR/GAMP5) implies strict screening.
Develop, configure, and qualify automation logic and historian integrations for DeltaV DCS systems in compliance with 21 CFR Part 11 and validation standards.
Create and manage DCS recipe parameters, formulas, and process flows according to tech transfer inputs, ensuring audit-ready documentation including DQ, IQ, OQ, and PQ.
Maintain traceability matrices, support software design document review, and integrate PI System architecture with MES, ERP, and SCADA systems for compliance and reporting.
Bachelor’s degree in Electrical and Electronics, Automation, Chemical or related engineering discipline.
Minimum 10 years of experience in automation engineering within a regulated industry (pharma/biotech preferred).
Strong working knowledge and hands-on experience with DeltaV DCS systems and Delta Batch Implementation (7016 or equivalent).
Work Location: On Premise.
Experienced engineer with deep expertise in regulated pharma/biotech automation environments handling DeltaV DCS and 21 CFR Part 11 compliant systems.
Proficient in developing and qualifying control logic, documentation per GAMP 5, and integration of PI System with industrial protocols and enterprise systems.
Open to leveraging AI tools for problem solving and productivity improvements with understanding of responsible AI usage.