• Principal Scientist - TS/MS API External…

    Lilly (Indianapolis, IN)
    …**Key Objectives/Deliverables:** + Provide technical oversight and stewardship for peptide and/or oligonucleotide manufacturing processes. + Leads resolution of ... drive continuous improvement with appropriate change controls in place. + Maintaining peptide /oligonucleotide processes in a state of compliance with US and global… more
    Lilly (10/07/25)
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  • Bioanalytical Scientist

    Eurofins US Network (Indianapolis, IN)
    …that will be beneficial: + Experience with biological sample preparation and peptide analysis using LC and mass spectrometry is highly desirable + Experience ... on Waters HPLC and Q-TOF instrument is beneficial + Technical proficiency in operation and troubleshooting of analytical instrumentation including chromatography and mass spectrometry **Additional Information** + Position is Monday-Friday 8:00am - 5:00pm… more
    Eurofins US Network (12/30/25)
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  • Analytical Development Scientist

    Eurofins US Network (Indianapolis, IN)
    …that will be beneficial: + Experience with biological sample preparation and peptide analysis using LC and mass spectrometry is highly desirable + Experience ... on Waters HPLC and Q-TOF instrument is beneficial + Technical proficiency in operation and troubleshooting of analytical instrumentation including chromatography and mass spectrometry **Additional Information** + Position is Monday-Friday 8:00am - 5:00pm… more
    Eurofins US Network (12/30/25)
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  • Advisor - Oligonucleotide Analytics

    Lilly (Indianapolis, IN)
    …high-resolution MS, oligonucleotide mapping, intact mass analysis, charge-variant analysis, peptide mapping) + Hands-on experience with operation, maintenance, and ... troubleshooting of analytical systems including UPLC, LC-MS, CE, MALS, SPR, and CD platforms + Familiarity with Agilent, Waters, and Thermo systems and associated software (eg, ChemStation, OpenLab CDS, BioConfirm, MassHunter, Chromeleon, BioPharma Finder,… more
    Lilly (12/20/25)
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  • Senior Director Quality Control

    Lilly (Lebanon, IN)
    …an advanced manufacturing facility for production of APIs (small molecule and peptide ) located in Lebanon, IN (Lilly Lebanon API). This facility is Lilly's ... largest investment in manufacturing capacity and is intended to provide 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… more
    Lilly (12/16/25)
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  • Sr. Director - Strategic Alliances (Smdd)

    Lilly (Indianapolis, IN)
    …high-quality supply of information and material for small molecule, peptide , and oligonucleotide assets. Responsibilities include: + _Implement and maintain ... strategic partnerships_ : Lilly's mission to bring novel therapeutics to patients begins in SMDD. This role will be instrumental to foster collaboration at external partners for the rapid design and development of drug substance and drug product for… more
    Lilly (12/16/25)
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  • Associate Director, Materials - Direct Materials…

    Lilly (Indianapolis, IN)
    …to ensure readiness for novel or custom materials often required in peptide or biologics manufacturing. _Process Excellence & Systems_ + Implement and refine ... processes to handle short lead-time orders, small batch sizes, and unique clinical material requirements. + Drive ERP/MRP enhancements to support the complexity of multiple modalities and accelerated production schedules. + Use Lean/Six Sigma principles to… more
    Lilly (12/12/25)
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  • Senior / Principal Process Engineer - APIEM

    Lilly (Indianapolis, IN)
    …world. **Position Brand Description:** The position of API EM Engineer _[Synthetic Peptide Synthesis and Purification]_ reports to the API EM Engineering Associate ... Director and provides technical leadership and expertise in conjunction with API EM contract manufacturer personnel in the reliable supply and commercialization of medicines with safety first and quality always by: + Developing and sustaining process knowledge… more
    Lilly (12/03/25)
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  • Senior Manager, CMC Global Regulatory Affairs

    Otsuka America Pharmaceutical Inc. (Indianapolis, IN)
    …The ideal candidate will also have some prior experience with biologic, peptide or oligonucleotide products. + Proven track record in late-stage development ... investigational filings, marketing applications (NDA/MAA), global submissions, and post-marketing lifecycle management as the CMC Regulatory lead. + Regulatory experience in handling-controlled substance applications will be a plus. **Skills:** + Comprehensive… more
    Otsuka America Pharmaceutical Inc. (12/02/25)
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  • Advisor/Sr. Advisor, Downstream Purification…

    Lilly (Indianapolis, IN)
    …clinical trials and commercialization for antibody-drug conjugates (ADCs), antibody- peptide conjugates (APCs), and antibody-RNA conjugates (ARCs/AOCs). We ... collaborate with our Synthetic Molecule Design and Development (SMDD), discovery, and biologics development colleagues to advance this exciting class of new drugs and seek fundamental learning and platform approaches to their development. **Position Summary:**… more
    Lilly (11/14/25)
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