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Peptide Synthesis Jobs in Indiana (NOW HIRING)

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Peptide Synthesis information

See Indiana salary details

$37K

$79.5K

$145.3K

How much do peptide synthesis jobs pay per year?

As of Aug 9, 2026, the average yearly pay for peptide synthesis in Indiana is $79,499.00, according to ZipRecruiter salary data. Most workers in this role earn between $62,808.00 and $84,369.00 per year, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in peptide synthesis, and why are they important?

To thrive in Peptide Synthesis, candidates typically need a strong background in organic chemistry or biochemistry, hands-on laboratory experience, and a relevant degree such as a B.S. or M.S. in chemistry or a related field. Proficiency with peptide synthesizers, analytical tools like HPLC and mass spectrometry, and adherence to laboratory safety protocols are commonly required. Attention to detail, problem-solving abilities, and effective communication skills help professionals work efficiently and accurately in a collaborative lab environment. These competencies are crucial for producing high-quality peptides, troubleshooting synthesis issues, and ensuring timely project delivery for research or pharmaceutical development.

What are the typical responsibilities and daily tasks of someone working in peptide synthesis?

Professionals in peptide synthesis are responsible for preparing, purifying, and analyzing synthetic peptides using specialized laboratory equipment. On a daily basis, they may set up and operate peptide synthesizers, perform quality control using techniques like HPLC and mass spectrometry, document results, and collaborate with research teams for process optimization. This role often involves troubleshooting synthesis challenges, maintaining laboratory supplies, and adhering to strict safety and quality standards. Working closely with other chemists or biologists, peptide synthesis specialists play a central role in supporting research, drug discovery, and development projects.

What is peptide synthesis?

A Peptide Synthesis job involves the chemical production of peptides, which are short chains of amino acids used in pharmaceuticals, research, and biotechnology. Professionals in this role operate specialized equipment, follow strict laboratory protocols, and ensure high-purity peptide production. They may also be responsible for troubleshooting synthesis issues, analyzing final products, and maintaining quality control standards. This role requires knowledge of organic chemistry, laboratory techniques, and peptide purification methods.

What are the most commonly searched types of Peptide Synthesis jobs in Indiana? The most popular types of Peptide Synthesis jobs in Indiana are:
Infographic showing various Peptide Synthesis job openings in Indiana as of August 2026, with employment types broken down into 75% Full Time, 22% Part Time, and 3% Contract. Highlights an 68% Physical, 4% Hybrid, and 28% Remote job distribution, with an average salary of $79,499 per year, or $38.2 per hour.

Scientific Director - Synthetic Process Chemistry (Peptides & Small Molecules)

Eli Lilly and Company

Indianapolis, IN • On-site

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

This job post has expired today. Applications are no longer accepted.


Eli Lilly and Company rating

8.8

Company rating: 8.8 out of 10

Based on 63 frontline employees who took The Breakroom Quiz

11th of 86 rated pharmaceutical


Job description

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 Synthetic Molecule Design and Development (SMDD) organization is responsible for the development of synthetic drug substances and drug products from the pre-clinical phase through commercialization. Our scientists and engineers develop innovative technical solutions to advance an existing portfolio that includes small molecules, synthetic peptides, oligonucleotides, and other emerging therapeutic modalities to help bring the next generation of life-changing medicines to patients.

Join the process chemistry team behind Mounjaro and Zepbound - two of the most impactful medicines in the world - and help shape the next generation of breakthroughs, including retatrutide, Lilly's first-in-class GIP/GLP-1/glucagon triagonist. An exciting opportunity is available for a highly skilled and experienced scientist with expertise in synthetic process chemistry to join SMDD at Eli Lilly and Company. You will be part of a dynamic, cross-functional department supporting one of the most productive peptide portfolios in the industry, spanning Discovery through Commercial phase, at the forefront of sustainable peptide development and commercialization.

Our core commercial strategy centers on traditional Liquid Phase Peptide Synthesis (LPPS) - applying small molecule-inspired fragment condensation chemistry to manufacture complex peptides like those found in Mounjaro and Zepbound at global scale. Sustainability is not an afterthought here - it is a strategic imperative embedded in everything we do, from reducing Process Mass Intensity (PMI) and eliminating hazardous reagents to publishing green chemistry innovations and leading industry-wide initiatives through the ACS GCI Pharmaceutical Roundtable and IQ consurtium. In this role, you will lead peptide commercialization projects built on this proven platform, championing greener process design at every stage. You will work closely with a growing team of chemists, analysts, and engineers to design synthetic routes, optimize condensation chemistry, and set a new standard for responsible peptide manufacturing.

This role operates in a highly collaborative environment with key partners across the United States, Asia, and Europe. Critically, this is a hands-on scientific role - the successful candidate will be expected to work at the bench alongside their team, not only direct from the sidelines. Technology developed in this role will feed directly into Lilly's Medicines Foundry, a state-of-the-art manufacturing facility coming online in Lebanon, Indiana within the next two years, giving this position rare end-to-end impact from laboratory discovery through commercial production.

Top candidates for this position will be expected to:

  • Serve as a hands-on scientific leader - personally conducting bench-level LPPS and condensation chemistry development while leading and mentoring a team of peptide chemists across commercial and pipeline programs.
  • Lead internal technology development and coordinate the transfer of early-phase processes to Lilly's Medicines Foundry (Lebanon, Indiana) - a next-generation facility supporting Phase 1 and 2 (and potentially Phase 3) clinical supply. For late-phase programs, collaborate with Lilly's internal and external Manufacturing groups to transfer processes for validation at internal facilities or external CMO partners.
  • Educate and guide CMO partners in best practices for greener peptide development and manufacture.
  • Engage with Lilly's Development and Manufacturing organizations to develop a deep understanding of new initiatives and drive continuous improvement in existing scientific processes.
  • Implement green chemistry and engineering solutions across all stages of process development - from solvent selection and reagent optimization to PMI benchmarking and publication of sustainability innovations in peer-reviewed journals and industry forums.
  • Present research findings at internal forums and external conferences; publish in high-quality, peer-reviewed journals.
  • Communicate technical and business-related implications of your work effectively to both scientific and non-scientific audiences.
Basic Qualifications:
  • Ph.D. in Chemistry or a closely related field with 7+ years of pharmaceutical industry experience in peptide or synthetic process chemistry; or M.S. with 10+ years of equivalent industry experience. The position level is flexible and will be commensurate with the successful candidate's experience - we welcome applications from early mid-career scientists through senior leaders with an established track record.
  • Demonstrated leadership in managing scientists and cross-functional project teams.
  • Experience with SPPS, LPPS, and/or hybrid peptide synthesis strategies at scale.
  • Experience with tech transfer of processes into manufacturing operations, including CMOs.
  • Track record of external publication and presentation in the peptide or synthetic chemistry field.
  • Strong communication skills, including the ability to present to both technical and business audiences.
Additional Preferences:
  • Excellence in multiple modes of peptide synthesis, including hybrid SPPS/LPPS and Tag-Assisted Liquid Phase Peptide Chemistry (TA-LPPS).
  • Experience with continuous flow chemistry, process intensification, or novel coupling reagent platforms.
  • Familiarity with regulatory CMC requirements for peptide drug substances.
  • Experience working with global CMO partners in Asia and/or Europe.
  • Strong interpersonal skills and a collaborative working style.
  • Demonstrated initiative, appropriate risk-taking, and ability to lead through ambiguity.
  • Knowledge and experience with management of technical projects across multiple programs.
  • Active participation in or awareness of professional societies and industry consortia relevant to pharmaceutical process chemistry and sustainability, including ACS, TIDES, the ACS Green Chemistry Institute Pharmaceutical Roundtable, and the IQ Consortium.
  • Demonstrated leadership capabilities, especially in cross-functional team environments.
  • Ability to prioritize multiple activities and influence others to promote a positive work environment.
Additional Information:
  • Position Location: Indianapolis, IN
  • The physical demands of this job are consistent with a laboratory environment.
  • Travel: 0 to 10% (domestic and international, including CMO and conference travel)

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.

Lilly is proud to be an EEO Employer and does not discriminate on the basis of age, race, color, religion, gender identity, sex, gender expression, sexual orientation, genetic information, ancestry, national origin, protected veteran status, disability, or any other legally protected status.


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 Network, Black Employees at Lilly, Chinese Culture Network, Japanese International Leadership Network (JILN), Lilly India Network, Organization of Latinx at Lilly (OLA), PRIDE (LGBTQ+ Allies), Veterans Leadership Network (VLN), Women's Initiative for Leading at Lilly (WILL), enAble (for people with disabilities). Learn more about all of our groups.

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

$148,500 - $257,400

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.

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About Eli Lilly

Sourced by ZipRecruiter

Eli Lilly, based in Indianapolis, IN, US, is one of the pioneers in the pharmaceutical industry with a rich history dating back to 1876. This global pharmaceutical company focuses on discovering, developing, manufacturing and selling pharmaceutical products in approximately 120 countries. The company's product categories include endocrinology, oncology, cardiovascular, neuroscience, and immunology. Having invested over $9 billion in research and development in the past decade, Eli Lilly is also committed to creating high-quality medicines that meet real needs. As a recipient of several awards and recognitions, Eli Lilly is known for its focus on life-saving research and drug development. Their mission is to make medicines that help people live longer, healthier, and more active lives.

Industry

Pharmaceutical product wholesalers

Company size

10,000+ Employees

Headquarters location

Indianapolis, IN, US

Year founded

1876