Eli Lilly and Company · 8 hours ago
Scientist – Lab Informatics, LabVantage Program - LIMS/LES
Indianapolis, IN
Full-time
Hybrid
Senior Level, Lead/Staff
$63K/yr - $163K/yr
5+ years expEli Lilly and Company is a global healthcare leader headquartered in Indianapolis, Indiana, dedicated to improving lives through innovative medicines. The Sr. Principal Associate – Lab Informatics will focus on standardizing business processes and workflows related to LIMS/LES systems to enhance the performance of manufacturing sites and quality control labs.
BiotechnologyHealth CareMedicalPharmaceutical
Responsibilities
The Sr. Principal Associate – Lab Informatics -LabVantage LIMS/LES Program is part of a team of informatics professionals who work closely with Tech@Lilly to identify, develop, validate, deploy, maintain, and defend globally owned, GMP compliant, informatics applications throughout their lifecycle. They represent the needs and interest of the business areas they support, and act as their voice and advocate
This position will focus on being the subject matter expert for LIMS/LES Systems by championing standardization of business processes, workflows, master data, and procedures globally to enable manufacturing sites and quality control labs to deliver world class performance. The candidate must consider the impacts of additional business processes that work with LIMS/LES such as other manufacturing and automation systems
The Sr. Principal Associate – Lab Informatics -LabVantage LIMS/LES Program is responsible for business processes owned, delivered, and maintained by the Quality Control function, including Test Execution, Data Documentation, Instrument Data Collection, Lab Inventory/Consumable Management, Equipment/Instrument Management, Lab Data Integrity, Data Review, and associated Test Automation and/or Master Data Management
Collaborate with business SMEs and stakeholders to define, develop and refine new business processes that promote the effective use of current and NextGen LIMS/LES applications
Develop and document Standard Operating Procedures (SOPs) for the application
Identify areas for improvement, propose, network, and implement potential solutions
Support deployment activities by guiding the sites on the “to be” processes on the NexGen solutions
Partner with third party application experts to find solutions to set up processes in the system or resolve issues
Advocate for users and stakeholders across the organization throughout requirements gathering and refinement of future release schedules
Identifying, refining, and standardizing global business requirements and business specific system configuration items, providing business input and guidance for system design decisions
Develop testing protocols and associated test scripts, authoring/editing validation deliverables, and execution/review of business-related validation test scripts
Participate in the execution of User Acceptance Testing (UAT) to ensure the application meets business requirements and quality standards
Document rational of business decisions to enable efficient progress, review, and historical reference
Knowledge in LIMS/LES master data and collaborate with the Global Data Stewards in the architecture of method built
Experienced in the master data elements related with instrument connectivity
Partner with global training representatives and third-party professional services teams to develop and maintain training materials
Work closely with global and local training professionals and third-party providers throughout this process to ensure effective delivery of the training regimen to site personnel
Provide ongoing support for LabVantage application including the reporting, management, and resolution of support issues
Coaching and mentoring of system users, sharing key learning and standard processes to the global LabVantage community to increase their system knowledge, and the identification of transferrable work processes between sites
The candidate will be part of the team that will provide answers to questions from inspections, audits, and other formal and informal assessments that impact globally owned applications and their associated workflows
Qualification
Required
Bachelor's Degree
5+ years of laboratory experience
Experience working in/with GMP laboratories
Strong scientific background
Clear understanding of quality laboratory issues and activities
Experience in defining and improving business processes
Knowledge of cGMP and quality systems
Proficient in quality documentation, control processes, and data integrity principles
Proven work with computer systems and their adaptability to existing business processes
Extensive knowledge of analytical methods, laboratory documentation and control processes
Knowledge of product release processes
Benefits
Company bonus
401(k)
Pension
Vacation benefits
Medical benefits
Dental benefits
Vision benefits
Prescription drug benefits
Flexible benefits
Life insurance
Death benefits
Certain time off and leave of absence benefits
Well-being benefits
Employee assistance program
Fitness benefits
Employee clubs and activities
Company
Eli Lilly and Company
We're a medicine company turning science into healing to make life better for people around the world.
10001+ employees
H1B Sponsorship
Eli Lilly and Company has a track record of offering H1B sponsorships. Please note that this does not
guarantee sponsorship for this specific role. Below presents additional info for your
reference. (Data Powered by US Department of Labor)
Distribution of Different Job Fields Receiving Sponsorship
Represents job field similar to this job
Trends of Total Sponsorships
2025 (514)
2024 (236)
2023 (167)
2022 (133)
2021 (57)
2020 (52)
Funding
Current Stage
Public CompanyTotal Funding
$6.5M2024-02-12Post Ipo Debt· $6.5M
1978-01-13IPO
Leadership Team
David Ricks
Chair, CEO
Lucas Montarce
Executive Vice President and Chief Financial Officer
Recent News
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