Senior Principal - HSE (Industrial Hygienist)

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 40,000 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 it 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 Houston, TX. 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 Houston 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. The Senior Principal Associate – Industrial Hygienist is a key member of the HSE team for a greenfield manufacturing site in Houston, Texas, providing site-wide technical leadership across project delivery, startup, and ongoing operations. This role is engaged early to influence facility and process design, engineering controls, containment strategies, and management of change requirements that protect employees and support compliant, reliable operations. The individual will also establish the foundational industrial hygiene programs, procedures, systems, and business processes needed for operational readiness and will serve as the site subject matter expert for industrial hygiene during routine operations. Responsibilities Lead site-wide industrial hygiene support for project design, construction, equipment selection, and startup activities to inform risk assessments, engineering controls, containment strategies, and management of change requirements for processes, equipment, and work environments. Develop and implement the site industrial hygiene framework, including written programs, procedures, exposure assessment strategies, governance processes, business processes, and training needed to support operational readiness and GMP manufacturing. Partner with project, engineering, operations, occupational health, maintenance, and quality stakeholders to identify industrial hygiene risks, implement practical control measures, and integrate requirements into site systems, startup plans, and safe work practices. Post-Startup Phase Oversee site industrial hygiene programs during operations, including exposure monitoring, medical surveillance support, respiratory protection, hazard communication, personal protective equipment, biological safety, and other applicable industrial hygiene programs, as well as required permits, reporting, and interactions with health and regulatory agencies, as applicable. Develop prioritized monitoring plans, interpret exposure and assessment data, prepare recommendations and reports, support audits and investigations, and track performance metrics to drive compliance, program effectiveness, and continuous improvement across the site lifecycle. Basic Qualifications Bachelor's degree required in industrial hygiene, occupational health, safety, engineering, chemistry, biology, environmental health, or a related scientific or technical discipline. 5+ years of relevant industrial hygiene and HSE experience within GMP manufacturing (pharmaceutical or chemical manufacturing preferred). 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 Certified Industrial Hygienist (CIH) certification preferred; candidates actively working toward certification may also be considered based on experience and qualifications. Previous experience supporting greenfield, startup, or major capital project environments in pharmaceutical, biotech, chemical, or other regulated manufacturing settings. Previous experience in cGMP pharmaceutical, biotech, or chemical manufacturing environments. Proficiency in industrial hygiene exposure assessment, air sampling strategy, data interpretation, and the application of engineering controls and containment concepts. Previous experience with respiratory protection, medical surveillance, hazard communication, personal protective equipment, biological safety, hazardous materials management, and applicable occupational health reporting requirements. Proven ability to influence cross-functional teams and provide sound technical recommendations during design reviews, risk assessments, and operational readiness planning. Additional Information Position Location: Houston, Texas Travel Percentage (%): Less than 5% annually. Shift Information: Primarily day shift; additional flexibility and occasional off-hours support may be needed during project delivery, startup, and ongoing site operations. 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 $101,250 - $169,400 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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