Sr. Automation Engineer, DeltaV

Technical Source is hiring for a Senior Automation Engineer who will support the design, oversight, and maintenance of the site’s DeltaV systems during commissioning. This role is focused on technical leadership, issue management, and project execution, rather than hands-on DeltaV coding.

Engineers in this role will act as a technical authority, ensuring quality, compliance, and schedule adherence during commissioning and SAT.

Key Responsibilities:

• Oversee and manage commissioning and Site Acceptance Testing (SAT) activities

• Independently identify, manage, and resolve project and system issues

• Review and sanity-check DeltaV coding and technical deliverables completed by other engineers

• Provide design recommendations based on project documentation and system requirements

• Lead problem-solving efforts during implementation, directing execution by other engineers as needed

• Support project execution including upgrades, system performance, vendor coordination, and DeltaV standards

• Interface closely with area representatives and commissioning / qualification teams

• Ensure equipment and systems are ready to meet project milestones and commissioning timelines

Qualifications:

Education:

• Bachelor’s degree in Engineering, IT, Science or related discipline is required.

Required:

• 5+ years of experience in a manufacturing environment, biopharmaceutical or pharmaceutical industry, or an equivalent combination of education and experience.

• Experience with DeltaV Batch Control and MES systems (Werum PAS-X strongly preferred)

• Strong knowledge of S95 Level 1 systems, including Emerson DeltaV, OSI Pi, PLCs, and IT Infrastructure

• Knowledge of industrial automation networks and communication protocols

• Understanding of S95 Level 4 systems, including ERP, Quality Systems, Data Warehouses, and CDL

• Working knowledge of ISA S95 and S88 standards and their application in global manufacturing

• Experience with OSI PI Historian and Werum MES

• Strong understanding of cGMP regulations, CSV, 21 CFR Part 11, and EU GMP Annex 11

• Proven background in Automation, Execution Systems, or IT roles within regulated manufacturing