Senior DeltaV Automation Engineer for GMP Startup

BioSpace; Houston (TX); On-site; USD 66,000 - 172,000; Full time

Job summary

Lilly Houston is hiring a Principal Automation Engineer to support the DeltaV DCS platform during startup of a new GMP manufacturing site. You will design, validate, and manage DeltaV systems and work with Quality, EPCs, and vendors.

The role requires 5+ years in Emerson DeltaV administration, strong Windows server experience, and a background in pharmaceutical manufacturing. Travel up to 20% may be required; relocation not stated.

Qualifications

• 5+ years of experience with Emerson DeltaV system administration.
• Experience with Windows servers and virtualization.
• Background in pharmaceutical manufacturing and CSV practices.
• Strong analytical, writing, and problem-solving skills.

Responsibilities

• Design, validate, and manage the DeltaV platform and site infrastructure.
• Lead system integration and OEM collaborations for DeltaV platforms.
• Develop computer system validation strategies and documentation.
• Support site procedures and capability building for automation team.

Skills

DeltaV administration

Windows Server

Process automation

Data integrity

Cross-functional collaboration

Education

Bachelor's degree in engineering or related Science Degree

Tools

Kneat Validation

Veeva Vault

Job description

Lilly Houston is hiring a Principal Automation Engineer to support the DeltaV DCS platform during startup of a new GMP manufacturing site. You will design, validate, and manage DeltaV systems and work with Quality, EPCs, and vendors.

The role requires 5+ years in Emerson DeltaV administration, strong Windows server experience, and a background in pharmaceutical manufacturing. Travel up to 20% may be required; relocation not stated.