Sr. Principal DeltaV Automation Engineer – Biotechnology
Eli Lilly and Company
Summary
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.
Job description
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. Post project delivery, this role will support GMP manufacturing operations in monoclonal antibodies or Bioconjugates.
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.
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.
Requirements
- Bachelor’s degree in engineering or related applicable discipline
- 5+ years of experience in Process Automation with Emerson DeltaV Platform
- 5+ years of experience in or supporting manufacturing
- Must be authorized to work in the United States on a full-time basis
- 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
Benefits
- 401(k) Matching
- Pension
- Vacation Benefits
- Medical, Dental & Vision
- Prescription Drug Benefits
- Flexible Spending Accounts
- Life Insurance
- Death Benefits
- Employee Assistance Program
- Fitness Benefits
- Employee Clubs and Activities
Company overview
Eli Lilly and Company, commonly known as Lilly, is a leading American multinational pharmaceutical corporation headquartered in Indianapolis, Indiana. Founded in 1876 by Colonel Eli Lilly, the company has grown into one of the world's most valuable pharmaceutical enterprises, with operations in approximately 125 countries. Lilly specializes in developing and manufacturing innovative medicines across multiple therapeutic areas, including diabetes, oncology, neuroscience, immunology, and cardiometabolic diseases. The company is renowned for its groundbreaking work in insulin production, having been the first to mass-produce insulin and later developing the first commercially available insulin product in the U.S. Lilly's current portfolio includes blockbuster medications such as Mounjaro and Zepbound (tirzepatide) for diabetes and obesity, Trulicity (dulaglutide) for type 2 diabetes, Verzenio (abemaciclib) for breast cancer, and Taltz (ixekizumab) for autoimmune conditions. With approximately 47,000 employees worldwide, Lilly maintains a strong commitment to research and development, investing heavily in scientific innovation to address some of the world's most significant health challenges. The company operates with a mission to make life better for people around the world through the discovery and delivery of innovative medicines.