Specialist - LDAR - Database Administrator

At Lilly, we unite caring with discovery to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to discover and bring life-changing medicines to those who need them, improve the understanding and management of disease, and give back to our communities through philanthropy and volunteerism. We give our best effort to our work, and we put people first. We’re looking for people who are determined to make life better for people around the world. Lilly is currently constructing an advanced manufacturing facility for production of API molecules located in Lebanon, IN. This facility is Lilly’s largest investment in manufacturing capacity and is intended to provide APIs for current and future products, including new modalities. This is a unique opportunity to be a part of the startup team for a greenfield manufacturing site, and the successful candidate will help to build the processes and systems to enable a successful startup into GMP manufacturing operations. Main Purpose and Objectives The LDAR Specialist is part of the LP1 HSE organization, working closely with the maintenance and operations teams. This role serves as the primary LDAR database administrator, responsible for building, maintaining, and optimizing the site’s LDAR database platform to ensure data integrity, accurate component tracking, and reliable monitoring route management. In addition to database administration, the LDAR Specialist provides technical support for the development, implementation, and improvement of the site LDAR program, helping to ensure regulatory compliance and minimize emissions. This role will be instrumental in establishing and managing the LDAR database management system, including reconciling process drawings with database records, creating and assigning monitoring routes, and maintaining accurate compliance data. The LDAR Specialist will also support the development of others responsible for utilizing the database and maintaining LDAR equipment and processes. As a greenfield site currently in its early stages, this role will evolve as the LDAR program matures - from initial database setup and configuration through steady-state data management and reporting. This is an opportunity to grow with the program. Key Responsibilities Assist in the development, implementation, and continuous improvement of the site LDAR program, including procedures, tools, and management systems Ensure compliance with EPA, IDEM, and cGMP regulatory requirements, including applicable NSPS (40 CFR Part 60) and NESHAP (40 CFR Part 63) subparts for pharmaceutical and chemical manufacturing Assist in conducting regular compliance audits to verify program effectiveness and regulatory adherence Serve as a secondary point of contact for regulatory agencies (EPA/IDEM) on LDAR-related matters, supporting the primary contact as designated by site HSE leadership Assist with emissions reduction initiatives through process optimization, equipment upgrades, and adoption of best practices Serve as the LDAR database administrator, including creation and assignment of monitoring routes Reconcile revised process drawings with the LDAR database, in collaboration with the LDAR Associate, to ensure accurate component counts Assist with maintaining accurate records of all LDAR-related activities, including monitoring data, repair logs, and compliance reports Assist with mentoring LDAR technicians and training operations and maintenance personnel on LDAR systems and procedures Assist with LDAR training programs in support of plant startup and ongoing team development Coordinate LDAR activities across production, operations, maintenance, engineering, and external vendors Support commissioning, qualification, and procedure writing related to LDAR systems Support cross-functional projects within Maintenance, Engineering, and Facilities teams Support incident investigations and ensure adherence to safety procedures, policies, and permits Assist with Method 21 LDAR monitoring as needed to meet regulatory monitoring schedule requirements Basic Requirements High school diploma required, technical certification or associate degree in environmental technology, instrumentation, or a related field preferred. Minimum 2 years of experience in pharmaceutical, chemical, refinery, petrochemical, or related industrial manufacturing with a focus on LDAR and environmental compliance Experience developing and/or managing LDAR programs Experience with environmental monitoring tools and software (e.g., LDAR database platforms) 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 Preferences Demonstrated knowledge of LDAR regulatory requirements (IDEM and/or EPA) and best practices Strong leadership and communication skills, with the ability to train, mentor, and coordinate across multiple teams and functions Project management experience Ability to lead cross-functional teams and drive continuous improvement Excellent problem-solving and troubleshooting skills Additional Information Tasks may require entering manufacturing areas and wearing appropriate PPE. May be required to provide support outside of normal working hours including nights, weekends, and holidays. Travel to other facilities within the Lilly network (minimal). As this is a greenfield site, the LDAR program will evolve from development to steady-state maintenance. This role may transform as LDAR capabilities mature at the site. 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 ( 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 Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women’s Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups. Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $28.84 - $42.31 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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