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Full Time Oligonucleotide Synthesis Jobs (NOW HIRING)

Agilent

Manufacturing Representative

Frederick, CO · On-site

$31.92 - $49.88/hr

Previous knowledge of oligonucleotide synthesis, HPLC, UF, conjugation, and lyophilization is ... The full-time equivalent pay range for this position is $31.92 - $49.88/hr plus eligibility for ...

Agilent

Manufacturing Representative

Frederick, CO · On-site

$31.92 - $49.88/hr

Previous knowledge of oligonucleotide synthesis, HPLC, UF, conjugation, and lyophilization is ... The full-time equivalent pay range for this position is $31.92 - $49.88/hr plus eligibility for ...

Eurofins

DNA Synthesis Technician I/II

Louisville, KY · On-site

Eurofins Genomics is looking for a DNA Synthesis Technician I/II to join our oligonucleotide ... Excellent full time benefits including comprehensive medical coverage, dental, and vision options

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Full Time Oligonucleotide Synthesis information

What is a full time oligonucleotide synthesis?

A Full Time Oligonucleotide Synthesis job involves the production and purification of short strands of DNA or RNA, known as oligonucleotides, in a laboratory setting. Professionals in this role use specialized equipment and chemical processes to synthesize oligos for research, diagnostics, or therapeutics. The position typically requires attention to detail, adherence to safety protocols, and maintaining accurate records. Full-time roles often also include responsibilities like quality control, troubleshooting instruments, and collaborating with other scientists.

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

To thrive as a Full Time Oligonucleotide Synthesis Specialist, you need a strong background in chemistry, molecular biology, and laboratory techniques, typically supported by a relevant bachelor's degree or higher. Familiarity with DNA/RNA synthesizers, HPLC, mass spectrometry, and laboratory information management systems (LIMS) is essential, along with any industry-standard certifications. Attention to detail, problem-solving abilities, and effective communication are standout soft skills in this role. These skills and qualifications ensure the accurate, efficient, and high-quality production of oligonucleotides critical for research and diagnostic applications.

What are some common challenges faced in a full time oligonucleotide synthesis role and how can they be managed?

A key challenge in full-time oligonucleotide synthesis is ensuring the precision and quality of each batch, as even minor errors can affect downstream research or clinical applications. Technicians often encounter issues such as instrument calibration, reagent purity, and troubleshooting failed syntheses. Staying organized, adhering to strict protocols, and maintaining detailed documentation are essential for managing these challenges. Collaboration with quality control teams and regular training on new synthesis technologies can also help mitigate common problems and improve overall workflow.

What is the difference between Full Time Oligonucleotide Synthesis vs Oligonucleotide Synthesis Technician?

AspectFull Time Oligonucleotide SynthesisOligonucleotide Synthesis Technician
CredentialsTypically requires a degree in chemistry, biochemistry, or related fieldUsually requires a diploma or associate degree in a relevant science
Work EnvironmentLaboratory setting, often in biotech or pharmaceutical companiesLaboratory or manufacturing environment, often in research labs
Job ResponsibilitiesDesign, synthesize, and analyze oligonucleotides; oversee synthesis processesPrepare and execute oligonucleotide synthesis; operate synthesis equipment

Full Time Oligonucleotide Synthesis roles generally involve more responsibility, including process oversight and design, while Oligonucleotide Synthesis Technicians focus on hands-on synthesis tasks. Both roles are essential in biotech labs, but Full Time positions often require more advanced education and experience.

What is the most common method of full time oligonucleotide synthesis?

Full time oligonucleotide synthesis typically uses solid-phase synthesis, where nucleotides are added sequentially to a growing chain attached to a solid support. This method allows for automation, high throughput, and precise control, making it the standard approach in the industry.
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Full Time Oligonucleotide Synthesis jobs near you
Infographic showing various Full Time Oligonucleotide Synthesis job openings in the United States as of August 2026, with employment types broken down into 1% Internship, 81% Full Time, 16% Part Time, and 2% Contract. Highlights an 71% Physical, 5% Hybrid, and 24% Remote job distribution.

Manufacturing Representative

Agilent

Frederick, CO • On-site

$31.92 - $49.88/hr

Full-time

Posted 14 days ago

Agilent Technologies rating

8.5

Company rating: 8.5 out of 10

Based on 43 frontline employees who took The Breakroom Quiz

33rd of 545 rated manufacturers

Job description

Job Description

As a Manufacturing Representative, you will check and schedule resources to ensure on-time delivery. Your scientific knowledge and background will be leveraged through your review of formulation documents and active ingredient dilution to ensure that products are manufactured to specification.

You will have an opportunity to become skilled in the use of a wide range of lab instruments, including but not limited to spectrophotometers, conductivity meters and auto-pipettors, all of which are critical to meeting our customers' requirements. Having the ability to learn quickly on the job, anticipate and resolve potential manufacturing and delivery issues and maintaining the highest level of quality are critical. Additionally, you will work on problems of diverse scope in which analysis of data requires evaluation of identifiable factors. You will also exercise judgment within generally defined practices and policies in selecting methods and techniques for obtaining solutions.

Key responsibilities include:

  • The manufacturing of oligonucleotide APIs in a GMP environment.

  • Actively involved in aspects of technology transfer and scale-up of oligonucleotide manufacturing processes delivered from Manufacturing Technical Services into Manufacturing.

  • Write and revise standard operating procedures according to regulatory and procedural guidelines.

  • Work with Validation and Engineering personnel to validate new equipment and facilities.

  • Work with Manufacturing Management and Quality to resolve manufacturing problems including drafting quality documentation (CAPA, deviation, change control, etc.).

  • Maintain, calibrate, and trouble shoot critical process equipment.

Shift Details:

The schedule will be Day shift (4:30am - 5:00pm) working a Pitman schedule: of 2 days working, 2 days off, 3 days working, 2 days off, 2 days working, then 3 days off.

Qualifications

  • Bachelor of Science Degree in related field or equivalent combination of education/experience

  • 1+ years of related manufacturing experience, pharmaceutical manufacturing environment preferred

  • Previous knowledge of oligonucleotide synthesis, HPLC, UF, conjugation, and lyophilization is advantageous

  • Detail-oriented and can perform technical duties following standard operating procedures and general laboratory safety rules

  • Clean room environment experience desired

  • Experience working in a FDA regulated manufacturing environment highly desired

Additional Details

This job has a full time weekly schedule. Applications for this job will be accepted until at least September 4, 2026 or until the job is no longer posted.The full-time equivalent pay range for this position is $31.92 - $49.88/hr plus eligibility for bonus, stock and benefits. Our pay ranges are determined by role, level, and location. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. During the hiring process, a recruiter can share more about the specific pay range for a preferred location. Pay and benefit information by country are available at: https://careers.agilent.com/locationsAgilent Technologies, Inc. is an Equal Employment Opportunity and merit-based employer that values individuals of all backgrounds at all levels. All individuals, regardless of personal characteristics, are encouraged to apply. All qualified applicants will receive consideration for employment without regard to sex, pregnancy, race, religion or religious creed, color, gender, gender identity, gender expression, national origin, ancestry, physical or mental disability, medical condition, genetic information, marital status, registered domestic partner status, age, sexual orientation, military or veteran status, protected veteran status, or any other basis protected by federal, state, local law, ordinance, or regulation and will not be discriminated against on these bases. Agilent Technologies, Inc., is committed to creating and maintaining an inclusive in the workplace where everyone is welcome, and strives to support candidates with disabilities. If you have a disability and need assistance with any part of the application or interview process or have questions about workplace accessibility, please email job_posting@agilent.com or contact +1-262-754-5030. For more information about equal employment opportunity protections, please visit www.agilent.com/en/accessibility.Travel Required: NoShift: DayDuration: No End DateJob Function: Manufacturing

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