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Analytical Method Development Scientist Jobs in Colorado

Electra

Scientist III, Analytical Chemistry

Boulder, CO · On-site

As a Scientist III, Analytical Chemistry on the Development team, you serve as a fully qualified ... Independently develop, validate, optimize, and execute analytical methods to support evolving R&D, ...

Electra

Scientist III, Analytical Chemistry

Boulder, CO · On-site

As a Scientist III, Analytical Chemistry on the Development team, you serve as a fully qualified ... Independently develop, validate, optimize, and execute analytical methods to support evolving R&D, ...

Magris Talc

Analytical Lab Scientist

Englewood, CO · On-site

$72K - $90K/yr

The Analytical Lab Scientist position is lab-based and will report to the Manager of Analytical ... Participate in method development and documentation. * Provide support to Quality and Product ...

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All JobsAnalytical Method Development Scientist JobsAnalytical Method Development Scientist Jobs in Colorado

Analytical Method Development Scientist information

See Colorado salary details

$23

$44

$68

How much do analytical method development scientist jobs pay per hour?

As of Jun 11, 2026, the average hourly pay for analytical method development scientist in Colorado is $44.24, according to ZipRecruiter salary data. Most workers in this role earn between $33.12 and $51.06 per hour, depending on experience, location, and employer.

What does an Analytical Method Development Scientist do?

An Analytical Method Development Scientist is responsible for designing, developing, and validating analytical methods used to test and analyze chemical compounds, pharmaceuticals, or other materials. They ensure that the methods are accurate, reliable, and compliant with regulatory standards. This role involves working with advanced laboratory instruments, troubleshooting analytical issues, and documenting procedures for use in research, quality control, or manufacturing environments.

What are the key skills and qualifications needed to thrive as an Analytical Method Development Scientist, and why are they important?

To thrive as an Analytical Method Development Scientist, a strong background in chemistry, analytical techniques, and method validation—often supported by a relevant degree in chemistry or pharmaceutical sciences—is essential. Familiarity with laboratory instrumentation such as HPLC, GC, MS, and software for data analysis, as well as knowledge of regulatory guidelines like ICH and FDA, is typically required. Attention to detail, problem-solving abilities, and effective communication are vital soft skills for success in this role. These skills ensure reliable method development, regulatory compliance, and effective collaboration within multidisciplinary scientific teams.

What are the typical challenges faced by an Analytical Method Development Scientist when transferring methods to quality control or manufacturing teams?

One common challenge for Analytical Method Development Scientists is ensuring that newly developed analytical methods are robust and reproducible when transferred to quality control or manufacturing teams. Differences in equipment, sample matrices, or operator technique can impact results, so thorough method validation and clear documentation are essential. Scientists often work closely with cross-functional teams to provide training, troubleshoot issues, and adapt protocols as needed. Successfully managing these transitions helps maintain product quality and regulatory compliance.

What is the difference between Analytical Method Development Scientist vs Analytical Chemist?

AspectAnalytical Method Development ScientistAnalytical Chemist
Primary FocusDeveloping and validating new analytical methodsPerforming routine analysis and testing
Work EnvironmentResearch labs, R&D departmentsQuality control labs, manufacturing facilities
CredentialsBachelor's or Master's in Chemistry or related field; experience in method developmentBachelor's degree in Chemistry or related field; experience in analytical testing

While both roles involve analytical testing, the Analytical Method Development Scientist primarily focuses on creating and validating new analytical methods, often in research settings. In contrast, the Analytical Chemist typically performs routine testing to ensure product quality in manufacturing or quality control labs.

What are popular job titles related to Analytical Method Development Scientist jobs in Colorado? For Analytical Method Development Scientist jobs in Colorado, the most frequently searched job titles are:
What job categories do people searching Analytical Method Development Scientist jobs in Colorado look for? The top searched job categories for Analytical Method Development Scientist jobs in Colorado are:
Analytical Method Development Scientist jobs near you
Infographic showing various Analytical Method Development Scientist job openings in Colorado as of June 2026, with employment types broken down into 99% Full Time, and 1% Part Time. Highlights an 85% Physical, 5% Hybrid, and 10% Remote job distribution, with an average salary of $92,028 per year, or $44.2 per hour.
Scientist, Analytical Development

Scientist, Analytical Development

Umoja Biopharma

Louisville, CO

$122K - $150K/yr

Other

Posted 10 days ago

Job description

POSITION SUMMARY

Umoja's Analytical Development organization is seeking a driven Scientist to deliver routine (U)HPLC as well as troubleshoot, improve and/or develop separations based analytical methods for the Process Analytics department.  This role will be responsible for managing current method lifecycle and developing new separation strategies to quantify residual process reagents, impurities in lentiviral vector (VivoVec) Drug Product and assist in product and process characterization. This position requires an exploratory and proactive approach to method development, including identifying and developing new separation methods to quantify residuals in VivoVec, raw materials, and media components to support evolving process needs, using appropriate chromatographic and detection strategies.

The ideal candidate is experienced in chromatography systems and multiple detection methods and will work independently to meet timelines. Responsibilities may include oversight and transfer of analytical assays for internal and external partners, qualification of newly developed or external methods, and successful transfer of methods to QC to enable release of GMP material. This role balances routine sample testing to support ongoing process needs with development, qualification, and transfer activities, and requires strong communication skills to collaborate with crossfunctional and external partners. Attention to detail, thorough documentation of experimental work in an Electronic Laboratory Notebook (ELN), and authorship of development and qualification reports are essential.

This role is fully onsite and lab-based 5 days/week at our Louisville, CO location.

CORE ACCOUNTABILITIES
Specific Responsibilities include:

  • Develop and execute novel (U)HPLC and separation methods to characterize and quantify lentiviral products, raw materials and impurities, including process reagents, to demonstrate effective clearance
  • Collaborate with AD and QC team members on various stages of analytical method lifecycle (development/qualification/transfer)
  • Collaborate with informatics engineers to create sample submission/result reporting workflows and integrate automation to support ongoing testing and improve efficiency.
  • Maintain clear records of experimental work using an electronic notebook system that adheres to company guidelines.
  • Manage and prioritize sample submissions for respective method(s) and report data in timely manner
  • Prepare technical data reports and presentations
  • Contribute to other analytical method(s) development and testing as necessary
  • Exemplify the company core values and adhere to company policies to ensure safety and quality of gene therapy products and facility.

The successful candidate will have:

  • PhD/MS/BS in Biology, Biochemistry, or related discipline with of relevant experience, respectively. Equivalent combination of education and experience will be considered.
  • Expertise with (U)HPLC systems and chromatography separation analytics, Thermo (Chromeleon) preferred with multiple separation and detection methods
  • Experience in novel method development and method improvement initiatives
  • Excellent communication skills with the proven ability to build open and collaborative relationships and successfully work as a member of a multidisciplinary team

Preferred Qualifications:

  • Expertise with nano and (U)HPLC
  • Experience with UV/VIS, Fluorescence, CAD, quadrupole MS, ICP-MS detection
  • Experience with viral vectors (e.g., AAV, LVV) and/or additional analytical methods (dPCR, qPCR, ELISA, etc.) a plus
  • Experience in method qualification and Quality transfer
  • Self-motivated and organized
  • Ability to work in a fast-paced environment, meet deadlines, and prioritize work on multiple projects

Physical Requirements

  • 100% compliance with personal protective equipment (PPE) requirements in laboratory environments, including gloves, protective clothing, and eye safety glasses.
  • Perform physical tasks required for the role, including standing, walking, bending, kneeling, sitting, working your hands in a biosafety cabinet, and occasionally moving materials up to 50 pounds.
  • Ability to work onsite 5 days/week at our Louisville, CO location.

Salary Range: $122,100 - $150,800

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