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Advisor - TS​/MS Lab - Lebanon API Manufacturing

Job in Lebanon, Boone County, Indiana, 46052, USA
Listing for: Eli Lilly and Company
Full Time position
Listed on 2026-01-15
Job specializations:
  • Healthcare
    Medical Science, Data Scientist
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

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 (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.

Job Summary

As a TSMS Lab Advisor at Eli Lilly and Company, you will be a key contributor to our Technical Services and Manufacturing Science (TSMS) team, providing expert scientific and technical guidance within our laboratory operations. You will ensure the highest standards of quality, compliance, and scientific rigor are maintained in support of our pharmaceutical manufacturing processes.

Job Responsibilities
  • Develop laboratory process and analytical expertise, provide technical oversight and stewardship for small molecule and peptide manufacturing
  • Design, oversee, and perform complex laboratory experiments, data analysis, and interpretation to support process development, characterization, and optimization.
  • Collaborate cross‑functionally with manufacturing, quality assurance, regulatory affairs, and research and development teams to resolve technical challenges and drive continuous improvement.
  • Provide scientific and technical leadership for troubleshooting activities related to manufacturing deviations and out‑of‑specification results.
  • Active role in mentoring and developing fellow TSMS laboratory scientists to facilitate tech transfer
  • Ensure compliance with all relevant internal procedures, external regulations (e.g., cGMP, FDA, ICH), and safety guidelines.
  • Stay abreast of industry trends, new technologies, and scientific advancements in pharmaceutical analysis and manufacturing.
Minimum Qualifications
  • Education:

    Master’s, or Ph.D. in Chemistry, Biochemistry, Analytical Chemistry, Pharmaceutical Sciences, or a related scientific discipline.
  • Master’s degree with 5+ years of relevant experience in a pharmaceutical or biotechnology laboratory setting OR Ph.D. with 2+ years of relevant experience in a pharmaceutical or biotechnology laboratory setting.
  • Expertise in small‑scale peptide and/or small molecule process development and scale‑up
  • Extensive hands‑on experience with advanced analytical techniques such as HPLC, GC, LC‑MS, GC‑MS, spectroscopy (UV‑Vis, FTIR), and dissolution testing.
  • Strong understanding of cGMP regulations, ICH guidelines, and pharmacopeial requirements (USP, EP, JP).
Additional Preferences
  • Proficiency in method development, validation, and transfer.
  • Experience with laboratory information management systems (LIMS) and chromatography data systems (CDS).
  • Excellent problem‑solving, critical thinking, and data analysis skills.
  • Strong written and verbal communication skills, with the ability to effectively present complex technical information.
  • Demonstrated ability to work independently and as part of a cross‑functional team.
  • Proven leadership abilities and experience mentoring junior staff.

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…

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