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Director Peptide Jobs (NOW HIRING)

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Director Peptide information

What does a director peptide do?

A Director of Peptide is a senior leader responsible for overseeing peptide research, development, and production within a biotechnology or pharmaceutical company. They manage teams working on peptide synthesis, optimization, and characterization to support drug discovery or manufacturing goals. Additionally, they develop strategic plans, ensure compliance with regulations, and collaborate with cross-functional teams to advance peptide-related projects from concept to market. Their role involves both scientific expertise and strong leadership skills to drive innovation and achieve business objectives.

How does a director peptide typically collaborate with cross-functional teams within a pharmaceutical organization?

A Director of Peptide often works closely with various departments such as research and development, manufacturing, regulatory affairs, and quality assurance. This collaboration ensures that peptide discovery, synthesis, and scale-up processes align with project timelines and regulatory requirements. The role frequently involves leading multidisciplinary project teams, facilitating communication between scientists and business stakeholders, and driving strategic decisions to advance peptide therapeutics from concept to clinical development.

What are the key skills and qualifications needed to thrive as a director peptide?

To thrive as a Director of Peptide, you need advanced expertise in peptide chemistry, drug development, and a PhD or equivalent experience in biochemistry or related fields. Familiarity with analytical instrumentation (e.g., HPLC, LC-MS), regulatory compliance systems, and project management software is typically required. Leadership, strategic thinking, and effective communication are crucial soft skills for guiding teams and cross-functional collaborations. These competencies ensure successful peptide project execution, innovation, and alignment with organizational goals in the pharmaceutical or biotech industry.
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Infographic showing various Director Peptide job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 13% Part Time, 1% Temporary, and 1% Contract. Highlights an 93% Physical, 2% Hybrid, and 5% Remote job distribution.

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

Initial Therapeutics, Inc.

Indianapolis, IN โ€ข On-site

$148.50 - $257.40/hr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted yesterday


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 lifeโ€‘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. Weโ€™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 preโ€‘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 lifeโ€‘changing medicines to patients.

Join the process chemistry team behind Mounjaroยฎ and Zepboundยฎ โ€” two of the most impactful medicines in the world โ€” and help shape the next generation of breakthroughs, including retatrutide, Lillyโ€™s firstโ€‘inโ€‘class GIP/GLPโ€‘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, crossโ€‘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) โ€” applying small moleculeโ€‘inspired fragment condensation chemistry to manufacture complex peptides like those found in Mounjaroยฎ and Zepboundยฎ at global scale. Sustainability is not an afterthought here โ€” 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 industryโ€‘wide initiatives through the ACS GCI Pharmaceutical Roundtable and IQ consortium. 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 handsโ€‘on scientific role โ€” 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 Lillyโ€™s Medicines Foundry, a stateโ€‘ofโ€‘theโ€‘art manufacturing facility coming online in Lebanon, Indiana within the next two years, giving this position rare endโ€‘toโ€‘end impact from laboratory discovery through commercial production.

Top candidates for this position will be expected to:
  • Serve as a handsโ€‘on scientific leader โ€” personally conducting benchโ€‘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 earlyโ€‘phase processes to Lillyโ€™s Medicines Foundry (Lebanon, Indiana) โ€” a nextโ€‘generation facility supporting Phase 1 and 2 (and potentially Phase 3) clinical supply. For lateโ€‘phase programs, collaborate with Lillyโ€™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 Lillyโ€™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 โ€” from solvent selection and reagent optimization to PMI benchmarking and publication of sustainability innovations in peerโ€‘reviewed journals and industry forums.
  • Present research findings at internal forums and external conferences; publish in highโ€‘quality, peerโ€‘reviewed journals.
  • Communicate technical and businessโ€‘related implications of your work effectively to both scientific and nonโ€‘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 candidateโ€™s experience โ€” we welcome applications from early midโ€‘career scientists through senior leaders with an established track record.
  • Demonstrated leadership in managing scientists and crossโ€‘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 Tagโ€‘Assisted Liquid Phase Peptide Chemistry (TAโ€‘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 riskโ€‘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 crossโ€‘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 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.

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

$148,500 - $257,400

Fullโ€‘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 companyโ€‘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 wellโ€‘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 Lillyโ€™s compensation practices and guidelines will apply regarding the details of any promotion or transfer of Lilly employees.

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