Sr. Principal DeltaV Automation Engineer - BiotechnologyLilly 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[redacted] (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[redacted] 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).
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). In addition, Lilly offers a comprehensive benefit program to eligible employees, including eligibility 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; and 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.
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