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.
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 35,000 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 (Lilly Lebanon API). 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 facility to enable a successful startup into GMP manufacturing operations.
Main Purpose and Objectives of Position:
The Environmental Advisor is part of the Lilly Lebanon API Health, Safety, and Environmental (HSE) team and provides technical leadership and expertise in the development, implementation, and maintenance of environmental programs, including supporting permitting efforts, where needed.
In the project delivery and startup phase of the project (startup expected 2025 to 2027), the HSE roles will be fluid and dynamic as we endeavor to support the project delivery, build a new organization, develop and implement the necessary systems and business processes required to support GMP operations, and build the site culture. This will require significant collaboration, creativity and resilience as the site grows to a full scale GMP manufacturing through start up.
Post start-up, this role will continue to be the be the subject matter expert (for assigned environmental programs) and provide oversight of operations of pharmaceutical API manufacturing units post-startup.
Key Responsibilities for this role include:
Develop and lead implementation of the operational readiness plan for the Lilly Lebanon API facility as a collaborative, inclusive, and energetic member of the HSE team. Examples of site environmental programs that this role may support include hazardous (RCRA) and non-hazardous waste, SPCC, DOT/Hazardous Materials, etc.Support the project team to deliver the facility as a key stakeholder providing input and feedback on environmental-related design decisions, construction, and startup plans while ensuring decisions meet project deliverables and compliance requirements, leveraging existing Lilly knowledge, and incorporating external experiences and learning.Develop and roll out environmental programs, procedures, tools, and overall management systems, including training, mentoring, and onboarding of new staff to help support a strong HSE culture at the site.Develop a partnership with Operations, Maintenance, and Engineering functions to help manage change, assure safety and compliance of new systems, and assist in setting requirements to assure safe and compliant startup.Ensure applicable internal and external reporting is coordinated and completed on time, including incorporating second person verification, as needed.Be a resource to the operational areas in helping them understand the regulatory requirements of their areas and programs; work with them in implementing solutions that comply with these regulations and programs. Facilitate the implementation of the programs and permits.Assure you the site is up to date with new or revised regulations and Lilly Global HSE standards.Complete internal HSE audits/assessments and lead/support incident investigations; support the development of long-term plans to drive program improvements.Availability to provide on-call support during weekends and after normal business hours.Additional Key Responsibilities:
Oversee the generation, transportation, treatment (if applicable), storage, and disposal of hazardous waste to ensure compliance with federal, state, and local regulations.Maintain accurate records of hazardous waste activities, including manifests, annual reports, and biennial reports as required by RCRA.Lead initiatives to reduce the generation of hazardous waste through process optimization, material substitution, and recycling programs.Conduct regular compliance audits and inspections to ensure adherence to hazardous waste regulations.Serve as the primary point of contact with regulatory agencies regarding hazardous waste management issues.Requirements:
Bachelor’s degree in environmental engineering, chemical engineering, chemistry, or related field of study5+ years of experience in pharmaceutical or chemical manufacturingExperience applying environmental regulations and developing environmental programsExperience interfacing with HSE-related regulatory agenciesAdditional Preferences:
Excellent organization and time management skills, as well as strong analytical skills and systematic and structured way of workingStrong collaboration and communication skillsAbility to lead cross-functional and technical teamsLilly 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.
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