Process Automation Engineer

i-Pharm GxP; Illinois; On-site; USD 90,000 - 120,000; Full time

Job summary

A leading life sciences consulting firm in Illinois seeks a Process Automation Lead to implement DeltaV automation for biopharmaceutical manufacturing. This role requires strong expertise in clean utilities and regulatory compliance. Ideal candidates will have a solid engineering background and strong project management skills, with a focus on delivering compliant and efficient operations.

Qualifications

• Proven expertise with Emerson DeltaV in pharmaceutical or biotechnology manufacturing.
• Strong understanding of GMP, GAMP 5, and regulatory compliance requirements.

Responsibilities

• Lead automation scope delivery for complex bioprocess systems.
• Oversee system integrator performance and deliverables.
• Manage and approve lifecycle documentation.

Skills

Expertise with Emerson DeltaV

Hands-on experience with automation for clean utilities

Understanding of GMP

Project management skills

Communication skills

Education

Bachelor’s degree in Engineering, Computer Science, or related field

Job description

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Specialist in US Contract and Project Delivery | Life Science GxP

Process Automation Lead (DeltaV – Biopharma Manufacturing)

12+ Month W2 Contract (Greencard or US Citizen Only) - No C2C or B2B

Our client is seeking an experienced Process Automation Lead to drive automation strategy and execution for advanced biopharmaceutical manufacturing. This role focuses on implementing and supporting DeltaV automation for Clean Utilities, ensuring robust, compliant, and efficient operations.

Responsibilities

• Lead automation scope delivery for complex bioprocess systems within Emerson DeltaV DCS.
• Oversee system integrator performance and deliverables, ensuring alignment with project scope, timelines, and quality standards.
• Manage and approve lifecycle documentation, including design specifications, configuration standards, and validation packages.
• Supervise and participate in software development, change management, and version control activities.
• Coordinate and execute Software FAT, Integration FAT, and Equipment FAT, ensuring seamless project delivery and regulatory compliance.
• Collaborate with engineering, validation, operations, and quality teams to ensure automation solutions support manufacturing and compliance needs.
• Provide technical leadership, troubleshooting, and guidance throughout the automation lifecycle.

Requirements

• Proven expertise with Emerson DeltaV in pharmaceutical or biotechnology manufacturing.
• Hands-on experience with automation for clean utilities.
• Strong understanding of GMP, GAMP 5, and regulatory compliance requirements.
• Experience managing system integrators and large-scale automation project delivery.
• Excellent communication, leadership, and problem-solving skills.
• Bachelor’s degree in Engineering, Computer Science, or related field (or equivalent experience).

Employment details

• Seniority level: Mid-Senior level
• Employment type: Contract

Industries

• Pharmaceutical Manufacturing, Biotechnology Research, and Business Consulting and Services

Note: This posting excludes C2C/B2B arrangements. Contact the employer for more details.