Senior Automation Engineer, DeltaV & GMP Startup

BioSpace

Houston (TX)

On-site

USD 66,000 - 172,000

Full time

11 days ago

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Benefits offered by this job

Company bonus

401(k) plan

Healthcare, dental, vision benefits

Job summary

Lilly is constructing an advanced manufacturing facility for API production in Houston. The Principal Automation Engineer – DeltaV System Administrator will join the site to design, validate, and manage DeltaV automation and related systems for GMP manufacturing startup.

The role requires 5+ years in DeltaV and pharma manufacturing, plus collaboration with QA, IT, and engineering teams. Occasional travel and a strong safety culture are emphasized as the project scales to full manufacturing

Qualifications

Bachelor’s degree in engineering or related science.
5+ years Emerson DeltaV administration experience.
Experience with Windows Servers and virtual environments.
5+ years of experience in pharmaceutical manufacturing.
Authorized to work in the United States on a full-time basis (no visa sponsorship).

Responsibilities

Design and deliver process automation systems including validation plans.
Support the design, delivery, validation, and system management of DeltaV platforms.
Lead system integrations and work with OEMs on DeltaV design and installation.
Develop site procedures related to computer system validation and administration practices.
Provide technical oversight for equipment and process system URs and design reviews.