Senior Advisor, Analytical Chemistry - Antibody-Drug Conjugates Linker Payload Development BR&D

Organization Overview

The Bioproduct Research and Development (BR&D) organization delivers new medicines to patients through the development and commercialization of insulins, peptides, oligonucleotides, monoclonal antibodies, novel therapeutic proteins, and gene therapy systems.

BR&D is a multidisciplinary group with deep technical expertise that works collaboratively with our discovery and manufacturing colleagues. Located in Indianapolis, IN, scientists have full access to Lilly's deep pharmaceutical development expertise and engineering capabilities. In this role, we are seeking experienced, innovative, and motivated candidates to apply their strong foundation in analytical sciences and experience in pharmaceutical development to enable clinical trials, regulatory submissions, and new product commercialization.

This role offers the opportunity to lead analytical development efforts focused on delivery of linker payload intermediate for antibody-drug conjugates within a multidisciplinary team while offering access to word-class capabilities for pharmaceutical development.

As an Advisor of Analytical Chemistry for Antibody-Drug Conjugates Linker Payload Development, you will play a pivotal role in driving innovation and ensuring scientific excellence within Lilly's development pipeline. You will be expected to foster interdisciplinary collaboration, leveraging cross-functional expertise to advance both early and late-stage ADC programs. Your leadership will influence strategic decision-making and contribute to Lilly's mission to transform patient outcomes worldwide.

Position Responsibilities

Top candidates for this position will be expected to

• Perform hands-on laboratory work to support the design, development, and implementation of analytical control strategies for small molecule and ADC payload linker programs, directly enabling clinical milestones and regulatory submissions.
• Lead and execute analytical development and commercialization efforts for the drug-linker intermediate used in antibody-drug conjugates (ADCs), including method development, qualification/validation, specification-setting, impurity/degradation characterization, reference standard management, and stability studies.
• Support and author technical reports and CMC sections for regulatory submissions and respond to health authority questions on analytical and product quality topics (IND/CTA, BLA/NDA/MAA, and country-specific RtQs).
• Collaborate with project teams to establish robust control strategies for linker-payload intermediates and process impurities, applying deep technical knowledge across linker/payload, mAb, and drug substance/product development.
• Drive technical and analytical strategies enabling linker-payload intermediate and conjugated DS/DP process design.
• Provide technical oversight for external analytical work, ensuring methods are scientifically sound and fit-for-purpose; lead technology transfer to CRO/CMO partners and internal Lilly sites.
• Mentor and develop junior team members, fostering technical growth and knowledge sharing.
• Introduce new analytical methodologies to advance ADC development and manufacturing.
• Plan and manage development timelines and resourcing; communicate progress and adjust plans as needed.
• Partner across Discovery, Development, and Manufacturing to deliver materials and data for clinical trials and regulatory filings.
• Bring strong communication, organizational, and leadership skills, and stay engaged with external innovation relevant to the ADC portfolio.

Basic Qualifications

• Ph.D. in Analytical Chemistry, Biochemistry, Chemistry, Organic Chemistry, Materials Sciences, Pharmaceutical Sciences, or a closely related STEM field; or
• M.S. in Analytical Chemistry, Biochemistry, Chemistry, Organic Chemistry, Materials Sciences, Pharmaceutical Sciences, or a closely related STEM field with 8+ years of relevant experience in the pharmaceutical industry experience; or
• B.S. in Analytical Chemistry, Biochemistry, Chemistry, Organic Chemistry, Materials Sciences, Pharmaceutical Sciences, or a closely related STEM field with 12+ years of relevant pharmaceutical industry experience.
• Strong expertise in analytical techniques such as IR, HPLC, GC, IC, LC/MS, KF, impurity profiling/structure elucidation, and method development, qualification/validation.

Additional Skills/Preferences

• Experience across multiple analytical techniques (e.g., HPLC, mass spectrometry, NMR, GC, KF etc.) and demonstration of strong hands-on laboratory skills and technical problem-solving abilities.
• PhD Candidates with >2 years of post-PhD hands-on laboratory experience in pharmaceutical or biopharmaceutical development or closely related analytical chemistry roles.
• Experienced candidates should demonstrate a track record of hands-on laboratory contributions to pharmaceutical development projects, including support of regulatory submissions (IND/NDA), method development and validation, and analytical testing strategies.
• Previous hands-on laboratory experience in the pharmaceutical industry or with analytical techniques directly applicable to pharmaceutical development (e.g., HPLC, MS).
• Deep fundamental understanding of and hands-on experience with reversed-phase, ion exchange, size-exclusion, chiral, and/or gas chromatography.
• Working knowledge and practical laboratory experience with optical spectroscopy (e.g., Raman, FTIR), NMR, structure elucidation.
• Strong hands-on technical skills, learning agility, ability to prioritize laboratory workload, and aptitude in navigating experimental challenges.
• Motivated to work both independently and collaboratively in a dynamic laboratory environment.
• Passion for applying analytical chemistry through hands-on laboratory work to solve real-world pharmaceutical development challenges and improve patient outcomes.
• Strong communication skills and ability to provide cross-functional leadership.
• Comfort managing multiple priorities.
• Demonstrated ability to drive change and generate creative, scientifically sound ideas for future work.

Additional Information

• Travel: 0 to 15%.
• Potential exposure to chemicals, allergens, and loud noises.
• Position is local and work is onsite in Indianapolis, IN at Lilly Technology Center-North (LTC-N).

Additional information

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 (AMECA), Black Employees at Lilly (BE@Lilly), Chinese Culture Network (CCN), EnAble, Evolve, Lilly Indian Network (LIN), Organization of Latinx at Lilly (OLA), Pride (LGBTQ+ Allies), Veterans Leadership Network (VLN) and Women's Initiative for Leading at Lilly (WILL).

Actual compensation will depend on a candidate's education, experience, skills, and geographic location. The anticipated wage for this position is $129,000 - $211,200

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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