Sr. Principal DeltaV Automation Engineer – Biotechnology

100 Eli Lilly and Company; Virginia (MN); On-site; USD 80,000 - 172,000; Full time

Benefits offered by this job

Company bonus

401(k)

Pension

Vacation benefits

Medical, dental, vision

Job summary

Lilly in Richmond, VA is seeking a Sr. Principal DeltaV Automation Engineer to lead the DeltaV platform delivery for a GMP monoclonal antibodies facility startup.

The role collaborates with cross-functional teams to design, qualify, and integrate automation systems for Drug Substance manufacturing. Responsibilities include leading DCS workstreams, coordinating system integrators, and developing validation strategies while supporting the GPACE automation program and site readiness ahead of

Qualifications

• Bachelor’s degree in engineering or related discipline.
• 5+ years of experience in Process Automation with experience on Emerson DeltaV Platform.
• 5+ years of experience in or supporting manufacturing.
• Authorized to work in the United States on a full-time basis.

Responsibilities

• Lead the design and delivery of the DeltaV platform and related software integration teams.
• Manage one or more system integrators for fully delivering and testing DeltaV software.
• Collaborate to deliver a fully integrated Automation/MES solution scaled to the business needs.
• Develop site automation processes and participate in validation strategies.

Skills

Automation engineering

Project leadership

Manufacturing experience

Collaboration

Education

Bachelor’s degree in engineering

Tools

DeltaV

MES

Job description

At Lilly, the work is demanding because patients are waiting. We unite caring with discovery to help make life better for people around the world, knowing that every decision, every detail, and every day matters. Headquartered in Indianapolis, Indiana, our over 50,000 employees around the globe take on complex challenges to discover and deliver life‑changing medicines, strengthen how health is understood and managed, and support the communities we serve. This is hard, urgent, selfless work—but it’s work worth doing. If you’re driven by purpose and ready to bring your best to work that truly matters for patients, we invite you to join us.

Sr. Principal DeltaV Automation Engineer – Biotechnology

Lilly is currently constructing an advanced manufacturing facility for production of monoclonal antibodies and bioconjugates located in Richmond, VA. This facility is intended to provide APIs for current and future products, including new modalities. This is a unique opportunity to be a part of the site technical team for the startup of a greenfield manufacturing site, and the successful candidate will help to build the organization, the facility and the culture to enable a successful startup into GMP manufacturing operations.

Responsibilities

The Sr. Principal Automation Engineer is a senior automation position that will lead the design and delivery of the DeltaV platform and associated software integration teams as part of Lilly’s manufacturing expansion. This role is intended to lead one or more project workstreams for the automation DCS function including design, scheduling, staffing, and qualification in the Drug Substance (Active Pharmaceutical Ingredient) network. During the design and delivery (startup expected 2029 to 2030) of the project this role will be integrated into the corporate delivery team leading one or more workstreams on the design, delivery, and startup of drug substance manufacturing focusing on monoclonal antibodies. This role will collaborate with A&E firms, system integrators, corporate and site engineering peers, and Tech@Lilly (Lilly’s corporate IT team) develop and manage the DeltaV DCS system and software design, testing, startup, and qualification. The Sr. Principal Automation Engineer is a site‑based position but will be closely integrated with Lilly’s Corporate Automation Team GPACE. GPACE (Global Process Automation & Control Engineering) provides automation, measurement, and process control solutions to Lilly manufacturing as well as a technical resource for training, standards, and capital project delivery. Post project delivery, this role will support GMP manufacturing operations in monoclonal antibodies or Bioconjugates. This will require significant collaboration, creativity and resilience as the site grows to a full scale GMP manufacturing through start up.

Key Deliverables

• Champion a strong safety culture, mentor and coach others, and utilize engineering and automation fundamental principles in design and problem solving.
• Collaborate with Lilly engineering, A&E firms, and system integrators to develop requirements and specifications that will be the foundation for software development and system architecture.
• Manage one or more system integrators for fully deliver and test DeltaV software.
• Collaborate with Tech@Lilly to deliver a fully integrated Automation/MES solution that is scaled for the needs of business.
• Participate in basic and detailed design that also includes staffing, statements of work, supplier management, and delivery strategies for automation systems.
• Participate in developing computer system validation strategies.
• Develop and build capabilities within the Richmond site automation team.
• Develop site procedures for automation platforms and associated administration activities.
• Provide engineering support for Process Safety Management (PSM) and Process Hazard Reviews (PHRs).
• Provide technical oversight during development of equipment and process system User Requirements and related Design Review/Qualification documentation to ensure equipment and systems are appropriate for intended purpose.

Basic Qualifications

• Bachelor’s degree in engineering or related applicable discipline required.
• 5+ years of experience Process Automation with experience on the Emerson DeltaV Platform.
• 5+ years of experience in or supporting manufacturing.
• Qualified applicants must be authorized to work in the United States on a full-time basis. Lilly will not provide support for or sponsor work authorization or visas for this role, including but not limited to F-1 CPT, F-1 OPT, F-1 STEM OPT, J-1, H-1B, TN, O-1, E-3, H-1B1, or L-1.

Additional Skills/Preferences

• Technical knowledge in process instrumentation.
• API/Drug Substance GMP manufacturing experience.
• Batch control.
• Strong analytical and critical thinking skills.
• Ability to collaborate with others.
• Ability to influence.
• Technical knowledge on the utilization of data historians.
• Experience with system integration including MES.

Additional Information

Potential for travel (less than 20% - could be domestic and/or international).

If you require accommodation to submit a resume for a position at Lilly, please complete the accommodation request form (https://careers.lilly.com/us/en/workplace-accommodation) for further assistance. Please note this is for individuals to request an accommodation as part of the application process and any other correspondence will not receive a response.

Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.

Our employee resource groups (ERGs) offer strong support networks for their members and are open to all employees. Our current groups include: Africa, Middle East, Central Asia (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women’s Initiative for Leading at Lilly (WILL).

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $79,500 - $171,600

• Full-time equivalent employees also will be eligible for a company bonus (depending, in part, on company and individual performance).
• eligible to participate in a company-sponsored 401(k)
• pension
• vacation benefits
• eligibility for medical, dental, vision and prescription drug benefits
• flexible benefits (e.g., healthcare and/or dependent day care flexible spending accounts)
• life insurance and death benefits
• certain time off and leave of absence benefits
• well-being benefits (e.g., employee assistance program, fitness benefits, and employee clubs and activities)

Lilly reserves the right to amend, modify, or terminate its compensation and benefit programs in its sole discretion and Lilly’s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.