Advisor/Sr. Advisor Automation, RNA Therapeutics
About this opportunity
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.
We are seeking an experienced Automation Engineer to design and implement robust automation platforms that integrate scientific instrumentation, robotic automation, and laboratory data management across Lilly’s RNA Therapeutics portfolio. This role reports to the Automation Lead for RNA Therapeutics and works within a multidisciplinary automation team responsible for delivering high throughput automated systems that increase the efficiency, reproducibility, and scalability of RNA therapeutic discovery workflows. The focus of this position is the design and implementation of automation platforms and integrated workcells rather than support of individual instruments, ensuring solutions are scalable, standardized, and deployable across multiple sites.
A key objective of this role is enabling Design Make Test Learn (DMTL) discovery cycles by implementing automation platforms that generate consistent, high quality experimental data with structured metadata capture. These platforms serve as experimental data generation infrastructure supporting downstream analytics and AI and machine learning model development. Automation platforms developed in this role will act as the experimental backbone of the RNA discovery DMTL cycle, enabling the generation of large, high quality datasets required to train and continuously improve AI and machine learning models.
Automation platforms developed in this role will support the generation of high-quality, standardized experimental datasets with consistent metadata capture, enabling reliable downstream analytics and machine learning model training.
The role requires deep expertise in liquid handling automation and experience implementing complex scientific workflows including next generation sequencing (NGS) library preparation and high throughput RNA processing. These automated workflows form a critical part of the infrastructure required to generate clean, reproducible, and unbiased datasets used to train machine learning models.
The successful candidate will partner closely with scientific, AI and ML, informatics, and data engineering teams to translate biological workflows into reliable automated platforms that produce traceable, structured experimental datasets. The ability to work in a collaborative, fast moving environment and adapt to evolving scientific needs is critical.
Responsibilities
Partner with internal partners to understand scientific workflows and develop automation solutions that improve throughput, reproducibility, data quality, and the generation of structured experimental datasets.
Design automation workflows that minimize experimental variability and bias while ensuring consistent metadata capture and traceability, enabling datasets suitable for downstream analytics and AI/ML model development.
Design, implement, and support laboratory automation platforms including liquid handlers, robotics, and integrated workcells from requirements gathering through deployment and scale up.
Lead implementation of complex automation platforms including RNA processing systems and next generation sequencing (NGS) library preparation workcells.
Develop robust liquid handling methods on Hamilton STAR liquid handling platforms including liquid class optimization, assay miniaturization, and workflow standardization.
Implement integrated automation workcells involving liquid handlers, plate handling robotics, and analytical instrumentation.
Contribute to the automation strategy and evolve solutions with business needs.
Find opportunities to improve reliability, efficiency, and scalability of existing automation platforms.
Implement complex integrated projects while proactively identifying risks and mitigation strategies and communicating progress to partners.
Work with Lab Operations and IT teams to plan space requirements, installation of automation hardware, and automation supply management.
Translate biological workflows into automation requirements including data capture, metadata tracking, experiment lineage and integration with digital systems.
Provide end user training and support for automation systems and digital laboratory platforms including ELN and LIMS systems such as Benchling to ensure consistent workflow execution and high quality experimental data capture.
Collaborate with interdisciplinary teams including scientists, hardware engineers, software engineers, informatics teams, data engineers, and data scientists.
Contribute to vendor selection and evaluation for automation hardware, software, and technology solutions.
Basic Requirements
BS in engineering or related field with 15+ years of pharma or biotech laboratory automation experience OR MS in engineering or related field with 10+ years of pharma or biotech laboratory automation experience, including demonstrated leadership in implementing complex automation platforms and delivering large scale automation systems.
Additional Skills/Preferences
Extensive experience designing and implementing laboratory automation solutions in an industry environment, including leading complex platform deployments and supporting production scale automation systems.
Deep hands-on experience designing, developing, and optimizing methods on Hamilton STAR liquid handling platforms, including authoring STAR methods, developing and tuning liquid classes, solving complex liquid handling behavior issues, and standardizing workflows across multiple systems or sites.
Experience implementing complex liquid handling methods including bead based workflows, assay miniaturization, and high precision pipetting.
Experience automating next generation sequencing (NGS) library preparation workflows including bead cleanup, normalization, and indexing PCR.
Experience implementing integrated automation workcells involving liquid handlers, robotics, and supporting analytical instrumentation.
Experience integrating automation systems with scheduling software such as Biosero Green Button Go.
Strong understanding of molecular biology workflows including RNA extraction, nucleic acid quantification, and sequencing workflows.
Experience integrating automation workflows with digital laboratory systems such as Benchling or similar ELN/LIMS platforms.
Experience developing automation requirements and documenting business processes.
Experience writing technical documentation including SOPs and automation specifications.
Fluency with Python or similar scripting languages.
Strong communication skills for technical and non technical audiences.
Demonstrated ability to manage multiple complex projects simultaneously in a collaborative environment.
Additional Information
This role may require up to 15 percent travel for training, conferences, or vendor visits.
The position is located in Boston, Massachusetts at the Lilly Genetic Medicine site in the Seaport district.
The role provides opportunities to mentor junior engineers and contribute to the evolution of the RNA automation platform across multiple sites.
Lilly is dedicated to helping individuals with disabilities to actively engage in the workforce, ensuring equal opportunities when vying for positions. 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
$141,000 - $228,800
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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Job details
How this role compares
Computed from every other active Manufacturing & CMC role in our database, not just this employer's listings.
We currently track 373 comparable Senior Manufacturing & CMC roles across 53 biopharma companies.
Salary context
174 of 373 peers report a salary range (USD, annualized)
Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.
Where these roles are based
Top locations among the 373 comparable roles
+ 14 more countries
Seniority mix
373 of 373 peers have a known seniority level
Therapeutic area mix
0 of 373 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden
No peers with a known therapeutic area yet.
Similar opportunities
The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.
How we calculate "similar"
No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.
Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.
0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.