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Senior Oligonucleotide Synthesis Jobs (NOW HIRING)

Senior Scientist, siRNA Synthesis

Worcester, MA · On-site

$91K - $124K/yr

Perform solid-phase oligonucleotide synthesis, deprotection, purification, and desalting of siRNA ... I or Senior Scientist II Additional Information Applicable only to applicants applying to a ...

Senior Scientist, siRNA Synthesis

Worcester, MA · On-site

$91K - $124K/yr

Perform solid-phase oligonucleotide synthesis, deprotection, purification, and desalting of siRNA ... or Senior Scientist II Additional Information ​Applicable only to applicants applying to a ...

Perform solid-phase oligonucleotide synthesis, deprotection, purification, and desalting of siRNA ... I or Senior Scientist II Additional Information Applicable only to applicants applying to a ...

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Senior Oligonucleotide Synthesis information

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$25K

$80.3K

$163.5K

How much do senior oligonucleotide synthesis jobs pay per year?

As of Aug 23, 2026, the average yearly pay for senior oligonucleotide synthesis in the United States is $80,287.00, according to ZipRecruiter salary data. Most workers in this role earn between $41,500.00 and $103,000.00 per year, depending on experience, location, and employer.

What is a senior oligonucleotide synthesis specialist?

Senior Oligonucleotide Synthesis specialists are experienced professionals who lead the design, production, and quality control of synthetic oligonucleotides—short DNA or RNA molecules used in research, diagnostics, and therapeutics. They manage and optimize automated synthesis processes, troubleshoot technical issues, and ensure the purity and accuracy of the final products. These specialists also train junior staff, maintain compliance with safety and regulatory standards, and often collaborate with research scientists to support advanced genetic studies and drug development.

What are the key skills and qualifications needed to thrive as a senior oligonucleotide synthesis specialist?

A Senior Oligonucleotide Synthesis Specialist requires expertise in organic chemistry, nucleic acid synthesis, and analytical techniques, typically backed by a degree in chemistry, biochemistry, or a related field. Familiarity with automated DNA/RNA synthesizers, HPLC, mass spectrometry, and relevant quality control systems is crucial. Attention to detail, strong problem-solving skills, and effective communication are essential soft skills for managing complex synthesis projects and collaborating with interdisciplinary teams. These competencies ensure the accurate production of high-quality oligonucleotides critical for research, diagnostics, and therapeutic applications.

What are some common challenges faced by senior oligonucleotide synthesis professionals, and how are they typically addressed in the lab environment?

Senior Oligonucleotide Synthesis professionals often encounter challenges such as optimizing reaction yields, troubleshooting complex instrumentation, and ensuring product purity and consistency. These challenges are typically addressed through rigorous protocol optimization, regular instrument maintenance, and close collaboration with analytical and quality control teams. Additionally, staying current with advancements in synthesis technologies and participating in cross-functional meetings help in proactively solving potential issues and maintaining high standards of productivity.

What is the difference between Senior Oligonucleotide Synthesis vs Oligonucleotide Synthesis Technician?

AspectSenior Oligonucleotide SynthesisOligonucleotide Synthesis Technician
CredentialsBachelor's or higher in chemistry or related field, experience in oligonucleotide synthesisAssociate degree or relevant technical training, less experience required
Work EnvironmentResearch labs, manufacturing facilities, overseeing synthesis processesHands-on synthesis work, equipment operation, quality checks
ResponsibilitiesDesign protocols, supervise synthesis, troubleshoot issuesPrepare reagents, operate synthesizers, perform routine quality control

In summary, Senior Oligonucleotide Synthesis roles involve higher-level responsibilities, supervision, and protocol development, while Oligonucleotide Synthesis Technicians focus on hands-on synthesis and equipment operation. Both roles are essential in the oligonucleotide manufacturing process but differ in experience requirements and scope of duties.

More about Senior Oligonucleotide Synthesis jobs

What cities are hiring for Senior Oligonucleotide Synthesis jobs?

Cities with the most Senior Oligonucleotide Synthesis job openings:

What are the most commonly searched types of Oligonucleotide Synthesis jobs?

The most popular types of Oligonucleotide Synthesis jobs are:

What states have the most Senior Oligonucleotide Synthesis jobs?

States with the most job openings for Senior Oligonucleotide Synthesis jobs include:

Infographic showing various Senior Oligonucleotide Synthesis job openings in the United States as of August 2026, with employment types broken down into 77% Full Time, 21% Part Time, and 2% Contract. Highlights an 65% Physical, 5% Hybrid, and 30% Remote job distribution, with an average salary of $80,287 per year, or $38.6 per hour.

Advisor/Senior Advisor - Oligonucleotide Chemistry

Eli Lilly and Company

Indianapolis, IN

$130K - $131K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 6 days ago


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.

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 49,000 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.

Lilly is passionate about the discovery, development and commercialization of potential new medicines that will impact and improve the lives of patients. Lilly Genetic Medicines is an innovation-focused organization striving to identify, develop and apply the most cutting-edge technologies to deliver maximum benefit to our patients. Our agile and diverse team strives to operate as an autonomous 'biotech-like' company within the walls of Lilly.

The Lilly Genetic Medicines (LGM) Team is looking for a collaborative, creative, and energetic problem solver to join a multidisciplinary team at the front edge of innovation. They will join our fast-paced, interdisciplinary team as we utilize novel RNA/oligonucleotide based therapeutic modalities to enhance the Lilly portfolio. The successful applicant will utilize their knowledge and technical expertise to accelerate the core capabilities of large-scale oligonucleotide synthesis of internal RNAi-based clinical candidates. Are you skilled in large-scale oligonucleotide synthesis and interested in learning about RNAi discovery and development for impactful patient therapies? We want you on our team!

Responsibilities:

  • Lead the Lilly Genetic Medicines discovery oligosynthesis scale-up team to accelerate Lilly RNAi Therapeutics from pre-clinical to clinical development
  • Utilize comprehensive expertise in oligonucleotide synthesis methodologies to support Lilly Genetic Medicines and further develop internal capabilities and team growth through effective coaching, mentorship, and leadership.
  • Collaborate with members of the RNAi discovery chemistry teams to validate and execute requirements for oligonucleotide synthesis from 150umol to 6mmol scales including communication of relevant information and results to project leads and/or cross functional organizations within Lilly to ensure seamless operation of the scale-up team.
  • Actively support our efforts toward the discovery of lead drug candidates and lead at the interface with our CMC and Development teams to provide essential materials for key studies and effectively communicate technical insights to the development team.
  • Demonstrate expertise in modern synthetic organic and nucleic acid chemistry, striving to improve methods, develop new technologies, and address synthetic oligonucleotide challenges across a diverse portfolio
  • Oversee and prioritize the work of scale-up team members to meet critical timelines.
  • Value diverse perspectives and experiences for effective solutions. Motivate team members to take initiative, own outcomes, and share expertise on complex technical challenges.
  • Guide teams through unclear situations, adapt efficiently to changes, and evaluate and implement effective approaches to completing tasks.

Basic Qualifications:

  • PhD degree in a relevant scientific discipline with 2+ years of experience (oligonucleotide synthesis experience, solid phase synthesis) or MS degree with 5+ years of experience (oligonucleotide synthesis experience, solid phase synthesis)

Preferred Qualifications:

  • Experience in supervising a team of scientists to evaluate, refine and execute synthetic routes, technologies, and practices to deliver LGM portfolio
  • Experience in troubleshooting and optimizing synthetic protocols on automated solid-phase synthesis instruments
  • Experience with downstream processing of oligonucleotides including use of chromatographic purification and process TFF systems
  • Ability to function within a highly interdisciplinary environment
  • Excellent written and oral communication skills, good organizational skills, the ability to multitask, and lead a team to deliver on tight deadlines
  • Confident, execution-focused, and team oriented with a desire to thrive in a fast-paced growing environment is a plus.
  • Strong laboratory skills and experience with analytical instrumentation such as AKTA, Agilent LC-MS and UPLC, Vanquish LTQ, Water's QDA, etc
  • Experience in developing new chromatographic methods (IEX/RP-HPLC, SPE, LC-MS).
  • Experience in conjugation of novel ligands, including small molecules, peptides, and proteins to oligonucleotides at 5-25g scale

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

$126,000 - $204,600

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

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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