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Director Peptide Synthesis Jobs in Indiana (NOW HIRING)

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Director Peptide Synthesis information

What does a director peptide synthesis do?

A Director of Peptide Synthesis oversees the research, development, and production of synthetic peptides within a laboratory or pharmaceutical setting. Their responsibilities include managing teams, ensuring quality control, optimizing synthesis protocols, and coordinating with other departments to meet project objectives. They also stay up-to-date on the latest advancements in peptide technology and regulatory requirements. This role requires strong leadership, technical expertise in peptide chemistry, and effective communication skills to drive successful outcomes.

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

To thrive as a Director of Peptide Synthesis, you need advanced knowledge in organic chemistry, peptide synthesis, and analytical techniques, typically supported by a Ph.D. in chemistry or a related field with significant leadership experience. Expertise with automated peptide synthesizers, HPLC, mass spectrometry, and familiarity with regulatory standards such as GMP is essential. Strong leadership, project management, and cross-functional communication skills help drive team performance and innovation. These competencies ensure high-quality peptide production, regulatory compliance, and the successful management of complex research or manufacturing operations.

What are some common challenges faced by a director peptide synthesis, and how can they be addressed?

A Director of Peptide Synthesis often encounters challenges such as managing complex projects with tight deadlines, ensuring high purity and yield in synthesis, and staying updated with rapidly evolving technologies. Balancing resource allocation across multiple teams and maintaining compliance with regulatory standards are also key concerns. These challenges can be addressed by fostering strong communication within multidisciplinary teams, investing in ongoing staff training, and implementing robust project management systems to streamline workflows and address issues proactively.

What is the difference between Director Peptide Synthesis vs Peptide Chemist?

AspectDirector Peptide SynthesisPeptide Chemist
CredentialsAdvanced degrees (PhD), extensive experience in peptide synthesisMaster's or PhD in chemistry or biochemistry
Work EnvironmentLeadership role overseeing teams and projects in labs or manufacturingHands-on laboratory research and synthesis work
Industry UsageUsed in biotech, pharmaceutical companies, and research institutionsCommon in research labs, pharmaceutical R&D, and academia

The main difference is that the Director Peptide Synthesis oversees and manages peptide synthesis projects and teams, focusing on strategy and leadership, while the Peptide Chemist conducts hands-on synthesis and research work. Both roles require strong chemistry credentials, but the director position emphasizes management and oversight.

What are popular job titles related to Director Peptide Synthesis jobs in Indiana?

For Director Peptide Synthesis jobs in Indiana, the most frequently searched job titles are:

What job categories do people searching Director Peptide Synthesis jobs in Indiana look for?

The top searched job categories for Director Peptide Synthesis jobs in Indiana are:

Researcher, Peptide Chemistry

Indiana Biosciences Research Institute Inc

Indianapolis, IN โ€ข On-site

Full-time

Medical, Life

Posted 19 days ago


Job description

IBRI is poised to transform life sciences-and for millions of people, even life itself.

The Opportunity:

The Researcher in Peptide Chemistry will support internal portfolio projects and external collaborative research activities through the synthesis, purification, and characterization of peptides. This laboratory-focused role includes maintaining instrumentation and reagent inventory, organizing and storing experimental data, and communicating results to relevant project teams. The position offers the opportunity for a candidate passionate about peptide synthesis to contribute directly to impactful drug discovery research while supporting high-quality laboratory operations, reliable documentation, and effective project execution.

Responsibilities:

  • Peptide Synthesis, Purification, and Characterization
  • Synthesize, purify, and characterize peptides in support of internal portfolio projects and sponsored research activities.
  • Execute peptide chemistry workflows with attention to quality, reproducibility, and project timelines.
  • Analyze and summarize peptide characterization data to support research decision-making.

Laboratory Instrumentation and Inventory

  • Maintain laboratory instrumentation to support ongoing peptide chemistry activities.
  • Monitor, organize, and maintain reagent inventory to ensure materials are available for project needs.
  • Coordinate routine laboratory upkeep and communicate maintenance or supply needs as appropriate.

Data Organization, Storage, and Communication

  • Organize, store, and maintain experimental data and documentation in accordance with project and laboratory expectations.
  • Communicate data, results, and project updates to relevant project teams in a clear and timely manner.
  • Support effective collaboration by ensuring accurate records and accessible data for internal stakeholders.

Qualifications:

  • Bachelor's degree in chemistry, biochemistry, chemical biology, pharmaceutical sciences, or a related field is required. Relevant experience may be considered in lieu of degree requirements.
  • At least 3 years of laboratory experience with automated and manual solid-phase peptide synthesis, purification, and/or characterization techniques.
  • Familiarity with HPLC purification and LC-MS analysis of synthetic peptides.
  • Ability to maintain accurate experimental records and organize data in a clear, accessible manner.
  • Experience with solid-phase peptide synthesis is highly.
  • Experience with preparative or analytical HPLC purification workflows.
  • Experience with peptide characterization using LC-MS, MS, or related analytical platforms.ย 
  • Ability to support laboratory operations, including instrumentation upkeep and reagent inventory management.
  • Exceptional organizational, communication, and collaboration skills.
  • Willingness to learn new techniques and support evolving project needs is essential.
  • Proficiency in Microsoft Office Suite.

Preferred Qualifications:

  • Experience with native chemical ligation protocols.
  • Experience with formulation of peptide drugs.
  • Experience maintaining laboratory instrumentation, reagent inventory, and organized data storage systems.
  • Experience supporting drug discovery research, collaborative research programs, and/or cross-functional project teams

Compensation:

Competitive salary and comprehensive benefits offered commensurate with experience.

About Us:

The Indiana Biosciences Research Institute (IBRI) is a first-in-class translational medicine institute dedicated to advancing life sciences in the race to eliminate disease and improve human health and life.

By connecting early-stage biotech companies with cutting-edge life science discoveries -and backed by the mission and resources of industry leaders, investors, and philanthropic partners-IBRI is successfully evolving a new, independent model to conquer disease, uniting previously fragmented forces in the quest for cures.

Carefully curating and supporting early-stage companies with investment, talent, and space, IBRI strategically accelerates drug discovery. Our work benefits from the relatively low cost of living and doing business here, allowing more resources to be directed toward science.

Fueled by the same entrepreneurial creativity as the groundbreaking scientific work we support, IBRI's labs advance research across the frontiers of diabetes, metabolic disease, Alzheimer's disease, and rare pediatric diseases. Our ambitious public-private vision cultivates talent while efficiently bridging the gap between research-driven inquiry and profit-driven drug development.

At IBRI, cures are launched on a clear pathway to clinical trials, enabled by the combined resources and experience of our academic and industry partners, without the typical pressure to deliver rapid results for commercialization. IBRI labs pursue breakthroughs that might never happen elsewhere. Breakthroughs are happening here. Our novel financing model ensures that when discoveries are ready for clinical trials, the intellectual property is sold back to industry or spun off, creating a direct stream of revenue.

By every measure, the IBRI model demonstrates a novel approach that delivers rewards. Scientific bench work is nurtured, drug discovery is advanced, workforce development is continuous, investors see returns, and donors see impact. Most importantly, IBRI's structure and portfolio of accomplishments matter to the patients whose lives are improved-or even saved-by this forward-looking approach to life sciences.

IBRI is driven to bring next-generation therapies to market with an understanding of the complex pressures that often bind innovation to economics. After more than a decade, the evidence is clear: IBRI is poised to transform life sciences-and for millions of people, even life itself.

Equal Employment Opportunity:

The IBRI provides equal employment opportunities to all employees and applicants and does not discriminate based on age, race, color, religion, gender, sexual orientation, gender identity, gender expression, national origin, protected veteran status, disability, or any other legally protected status.