BioSpace
Sr. Principal Analytical Scientist - TS/MS Lab - Lebanon API Manufacturing
BioSpace, Lebanon, Indiana, United States, 46052
Sr. Principal Analytical Scientist - TS/MS Lab - Lebanon API Manufacturing
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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 work to discover and bring life‑changing medicines, improve disease understanding and management, and give back through philanthropy and volunteerism. We put people first and seek individuals who are determined to make a difference worldwide.
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 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 Eli Lilly and Company seeks a highly experienced Senior Principal Analytical Scientist to lead critical analytical development and support activities within the Technical Services and Manufacturing Sciences (TSMS) Lab. This role will advance Eli Lilly’s pipeline by providing expert analytical oversight, troubleshooting complex issues, and driving the implementation of cutting‑edge analytical technologies to ensure product quality and process understanding.
Job Responsibilities
Serve as a subject‑matter expert in analytical science, providing strategic direction and technical leadership for complex analytical projects within the TSMS Lab.
Lead the design and development of complex LC‑MS methods for the identification, quantification, and characterization of small molecules and peptides in support of API commercial manufacturing.
Independently lead deviation investigations and process optimization initiatives using analytical methodologies, especially LC/MS.
Proactively identify, evaluate, and implement new analytical technologies and instrumentation to enhance capabilities, improve efficiency, and support API manufacturing.
Ensure all analytical activities are conducted in accordance with cGMP, ICH, and other relevant regulatory guidelines.
Collaborate effectively with cross‑functional teams including process development, manufacturing, quality control, and regulatory affairs; mentor and provide technical guidance to junior scientists and laboratory personnel.
Critically analyze and interpret complex analytical data, generating comprehensive reports and presentations to communicate findings and recommendations to stakeholders.
Maintain meticulous laboratory notebooks, author analytical method documentation, and technical transfer documents.
Minimum Qualifications
Education: Ph.D. in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, or a closely related discipline with at least 10 years of relevant experience in the pharmaceutical or biotechnology industry; OR a Master’s degree with at least 12 years of relevant experience; OR a Bachelor’s degree with at least 15 years of relevant experience.
Technical Expertise: Extensive hands‑on experience and deep theoretical understanding of a broad range of analytical techniques, including chromatography (HPLC, GC, UPLC), mass spectrometry (LC‑MS/MS, GC‑MS), spectroscopy (UV‑Vis, FTIR, Raman), and other relevant physiochemical characterization methods.
Regulatory Knowledge: In‑depth knowledge of cGMP, ICH guidelines, and other global regulatory requirements pertaining to analytical method development, validation, and quality control.
Additional Preferences
Problem‑Solving Skills: Demonstrated ability to independently troubleshoot complex analytical challenges, conduct OOS investigations, and implement effective solutions.
Leadership & Mentorship: Proven ability to provide technical leadership, mentor junior scientists, and influence technical direction within a team or project.
Communication Skills: Excellent written and verbal communication skills, with the ability to present complex scientific information clearly and concisely to diverse audiences.
Collaboration: Strong interpersonal skills with a proven ability to collaborate effectively in a cross‑functional team environment.
Innovation: Demonstrated track record of identifying and implementing new analytical technologies or approaches to solve scientific problems.
Lilly is dedicated to helping individuals with disabilities actively engage in the workforce, ensuring equal opportunities. 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. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, transgender status, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $66,000 – $171,600. Full‑time employees also are eligible for a company bonus (depending on company and individual performance) and a comprehensive benefits program including 401(k), pension, vacation, medical, dental, vision, flexible spending accounts, life insurance, leave of absence, and well‑being benefits.
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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 work to discover and bring life‑changing medicines, improve disease understanding and management, and give back through philanthropy and volunteerism. We put people first and seek individuals who are determined to make a difference worldwide.
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 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 Eli Lilly and Company seeks a highly experienced Senior Principal Analytical Scientist to lead critical analytical development and support activities within the Technical Services and Manufacturing Sciences (TSMS) Lab. This role will advance Eli Lilly’s pipeline by providing expert analytical oversight, troubleshooting complex issues, and driving the implementation of cutting‑edge analytical technologies to ensure product quality and process understanding.
Job Responsibilities
Serve as a subject‑matter expert in analytical science, providing strategic direction and technical leadership for complex analytical projects within the TSMS Lab.
Lead the design and development of complex LC‑MS methods for the identification, quantification, and characterization of small molecules and peptides in support of API commercial manufacturing.
Independently lead deviation investigations and process optimization initiatives using analytical methodologies, especially LC/MS.
Proactively identify, evaluate, and implement new analytical technologies and instrumentation to enhance capabilities, improve efficiency, and support API manufacturing.
Ensure all analytical activities are conducted in accordance with cGMP, ICH, and other relevant regulatory guidelines.
Collaborate effectively with cross‑functional teams including process development, manufacturing, quality control, and regulatory affairs; mentor and provide technical guidance to junior scientists and laboratory personnel.
Critically analyze and interpret complex analytical data, generating comprehensive reports and presentations to communicate findings and recommendations to stakeholders.
Maintain meticulous laboratory notebooks, author analytical method documentation, and technical transfer documents.
Minimum Qualifications
Education: Ph.D. in Analytical Chemistry, Biochemistry, Pharmaceutical Sciences, or a closely related discipline with at least 10 years of relevant experience in the pharmaceutical or biotechnology industry; OR a Master’s degree with at least 12 years of relevant experience; OR a Bachelor’s degree with at least 15 years of relevant experience.
Technical Expertise: Extensive hands‑on experience and deep theoretical understanding of a broad range of analytical techniques, including chromatography (HPLC, GC, UPLC), mass spectrometry (LC‑MS/MS, GC‑MS), spectroscopy (UV‑Vis, FTIR, Raman), and other relevant physiochemical characterization methods.
Regulatory Knowledge: In‑depth knowledge of cGMP, ICH guidelines, and other global regulatory requirements pertaining to analytical method development, validation, and quality control.
Additional Preferences
Problem‑Solving Skills: Demonstrated ability to independently troubleshoot complex analytical challenges, conduct OOS investigations, and implement effective solutions.
Leadership & Mentorship: Proven ability to provide technical leadership, mentor junior scientists, and influence technical direction within a team or project.
Communication Skills: Excellent written and verbal communication skills, with the ability to present complex scientific information clearly and concisely to diverse audiences.
Collaboration: Strong interpersonal skills with a proven ability to collaborate effectively in a cross‑functional team environment.
Innovation: Demonstrated track record of identifying and implementing new analytical technologies or approaches to solve scientific problems.
Lilly is dedicated to helping individuals with disabilities actively engage in the workforce, ensuring equal opportunities. 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. Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, transgender status, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.
Actual compensation will depend on a candidate’s education, experience, skills, and geographic location. The anticipated wage for this position is $66,000 – $171,600. Full‑time employees also are eligible for a company bonus (depending on company and individual performance) and a comprehensive benefits program including 401(k), pension, vacation, medical, dental, vision, flexible spending accounts, life insurance, leave of absence, and well‑being benefits.
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