DeltaV Automation Engineer - Pharma Tech Curriculum

QCS Staffing; Kentucky; On-site; USD 90,000 - 120,000; Full time

Job summary

QCS Staffing seeks an Automation Engineer specialized in Technical Curriculum for a major pharmaceutical project in Ohio. The role focuses on configuring DeltaV systems, developing batch solutions per ISA-88, and delivering operator graphics with best practices.

You will engage in commissioning, validation, and continuous improvement within a GMP environment. Ideal candidates will have hands-on DeltaV credentials, familiarity with GAMP 5 and 21 CFR Part 11, and the ability to create

Qualifications

• DeltaV v16 (or v15) configuration and engineering experience.
• GMP regulated pharmaceutical or biotech manufacturing experience.
• Instructors with hands-on DeltaV engineering credentials.
• Familiarity with GAMP 5, 21 CFR Part 11, and data integrity principles.
• Ability to develop site-specific content from customer configuration, recipes, and graphics.
• Ability to comply with safety and security requirements; onsite work as required.

Responsibilities

• Engineer and configure DeltaV control system architecture, hardware and network infrastructure.
• Develop control modules and automation strategies using function blocks, PID control, SFCs, interlocks and permissives.
• Create and maintain batch solutions in line with ISA-88, including phase logic and recipe development.
• Design DeltaV Live graphics and operator interfaces following ISA-101 best practices.
• Configure field devices and system communications, including Ethernet protocols.
• Support commissioning, validation, troubleshooting and continuous improvement projects.

Tools

DeltaV GSC / DeltaV software

ISA-88 / DeltaV Batch

DeltaV Live Graphics Studio

GAMP 5

21 CFR Part 11

ALCOA+ data integrity

Job description

QCS Staffing seeks an Automation Engineer specialized in Technical Curriculum for a major pharmaceutical project in Ohio. The role focuses on configuring DeltaV systems, developing batch solutions per ISA-88, and delivering operator graphics with best practices.

You will engage in commissioning, validation, and continuous improvement within a GMP environment. Ideal candidates will have hands-on DeltaV credentials, familiarity with GAMP 5 and 21 CFR Part 11, and the ability to create