Principal Automation Engineer, CSV – Pharma Manufacturing

100 Eli Lilly and Company

Richmond (VA)

On-site

USD 68,000 - 174,000

Full time

11 days ago

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Job summary

Lilly is building a next-generation biotech drug substance manufacturing facility in Richmond, VA, seeking a Principal Automation Engineer – CSV. The role requires deep knowledge of process automation, CSV practices, and data integrity within a cGMP pharmaceutical environment.

You will design and deliver CSV plans, collaborate across Quality and Engineering, and lead a contingent workforce to support multiple project streams while ensuring compliance and robust documentation.

Qualifications

Bachelor’s degree required.
3+ years of experience in computer system validation and process automation for manufacturing.
Authorized to work in the United States full-time.

Responsibilities

Champion a safety culture and mentor others in design and problem solving.
Develop CSV plans and validation strategies for process automation (DCS/PLC).
Collaborate with Lilly Quality, Corporate Engineering and partners on qualification testing.
Lead contingent workforce to support multiple project delivery streams for CSV.
Ensure CSV documents meet Quality Standards and regulatory templates.
Assist in design staffing, supplier management and delivery strategies for validation.
Build capabilities within the Richmond site automation team.
Support site procedures related to CSV and administration practices.
Provide technical oversight for URs and Qualification documentation.