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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.

The Bioanalytical Research Group (BAR) in Investigative ADME/Toxicology and BioAnalytical Research at Louisville, CO is seeking an expert scientist skilled in small and large molecule mass spectrometry to deliver innovative ways to support Lilly’s oncology portfolios. This role has an emphasis on bioanalysis of small molecule drug, especially radioligand therapeutics (RLT), with the possibility to expand into antibody-drug conjugates (ADC).

• Perform sample preparation (e.g. tissue homogenization, multiwave digestion, immunoaffinity enrichment, protein precipitation) and operate mass spectrometer to develop bioanalytical methods and perform quantitative bioanalysis (bioA) of small molecule or/and large molecule therapeutics from in‑vitro and in‑vivo samples.
• Investigate the structure‑activity relationship (SAR) including pharmacokinetics (PK), biodistribution (bioD), biotransformation (BioT) and metabolite identification (metID) of drug molecules using LC‑MS/MS.
• Collaborate with ADME project leaders to support fast‑paced drug discovery projects. Serve as bioA representative and provide bioanalytical expertise to project team.
• Mentor junior scientists in developing their skills in LC‑MS sample preparation, data analysis, visualization and reporting.
• Maintain and troubleshoot lab instruments to ensure their operation.

• Bachelor’s degree in science or engineering (chemistry, chemical engineering, bioengineering or related field) with at least 7 years of work experience, or master’s degree in related field with at least 5 years of work experience.
• Experience with using inductively coupled plasma (ICP), triple quadrupole (QQQ), high‑resolution mass spectrometer (HRMS, including QToF, Orbitrap) in bioA method development, qualification, and transfer.
• Experience with small and large molecule bioanalysis, including sample preparation (e.g. tissue homogenization, microwave assisted acid digestion), sample extraction (LLE, SPE, immunoprecipitation, protein precipitation) prior to MS.
• Experience of drug ADME principles in understanding PK, biodistribution and biotransformation of small and large molecule therapeutics.
• 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.

• Experience with discovery and development of radioligand therapeutics and elemental analysis using Agilent 8900 ICP‑MS. Hands‑on experience in sample preparation, LC‑MS bioanalytical workflow to support the bioA and metID of RLTs.
• Familiar with bioanalytical workflow of biotherapeutics (mAbs, ADC, siRNA, fusion protein, etc.), including immunoprecipitation, proteolytic digestion and deglycosylation. Bottom‑up peptide, payload quantification using Sciex 6500/7500. Intact mass acquisition, top‑down MS using Thermofisher Orbitrap Exploris 240/480/Tribrid instruments.
• Familiar with MS‑related informatic tools to conduct in‑depth data analysis – Mass Hunter, Biopharma Finder, QuantBrowser, MultiQuant, Biologics Explorer, Protein Metrics, MassMetaSite, etc. AI‑based data analysis and report writing are an advantage.
• Previous experience in experiment documentation (eLN, signals, benchling, etc.), PK calculation (Phoenix, Watson LIMS, R‑studio aNCA), data visualization (PRISM, BioRender) and report QC.
• Hands‑on experience in automation instruments, such as Apricot, Hamilton, Tecan and KingFisher to support high‑throughput bioanalytical assays.

Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $71,250 - $213,400.

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.

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 (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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