ZipRecruiter

Log In

1

Analytical Method Development Scientist Jobs in New York

Neion Bio

Scientist, Analytical Development

New York, NY · On-site

$130/hr

Working alongside our process development scientists, this individual will develop and implement ... Develop, optimize, and perform selected analytical methods in-house, including assays for protein ...

Neion Bio

Scientist, Analytical Development

New York, NY · On-site

$130/hr

Working alongside our process development scientists, this individual will develop and implement ... Develop, optimize, and perform selected analytical methods in-house, including assays for protein ...

next page

Showing results 1-20

All JobsAnalytical Method Development Scientist JobsAnalytical Method Development Scientist Jobs in New York

Analytical Method Development Scientist information

See New York salary details

$24

$46

$71

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

As of Aug 6, 2026, the average hourly pay for analytical method development scientist in New York is $46.03, according to ZipRecruiter salary data. Most workers in this role earn between $34.47 and $53.12 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?

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 New York? For Analytical Method Development Scientist jobs in New York, the most frequently searched job titles are:
What job categories do people searching Analytical Method Development Scientist jobs in New York look for? The top searched job categories for Analytical Method Development Scientist jobs in New York are:
Analytical Method Development Scientist jobs near you
Infographic showing various Analytical Method Development Scientist job openings in New York as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, and 3% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution, with an average salary of $95,749 per year, or $46 per hour.

Scientist, Analytical Development

Neion Bio

New York, NY

$130/hr

Full-time

Medical, Dental, Vision, Retirement

Re-posted 21 hours ago

Job description

About Neion Bio

Neion Bio is harnessing nature's best molecular factory, the chicken egg, to make medicine affordable, accessible, and resilient. We turn farms into medicine factories using cutting edge genetic engineering and stem cell technology. These "living bioreactors" are fully autonomous 3D biomolecular printers that operate on existing industrial-scale infrastructure. Our platform can rapidly and scalably produce almost any protein, provide national resilience to drug shortages and de-risk complex supply chains, and ultimately take advantage of novel biological environments to solve unmet medical needs. Biomanufacturing, reinvented. Medicine, democratized.

Role Summary

We are looking for a talented analytical scientist to lead analytical development and product characterization for monoclonal antibodies and other biologics produced using Neion Bio's platform.

Working alongside our process development scientists, this individual will develop and implement analytical strategies to characterize product quality, guide process development, and support comparability, technology transfer, and regulatory submissions. The role will span physicochemical, structural, and functional characterization, including glycosylation, purity and aggregation, binding, and potency assays. The successful candidate will be responsible for in-house development and managing external programs. 

Key Responsibilities

  • Develop and execute analytical strategies for monoclonal antibodies and other therapeutic and non-therapeutic proteins from early development through clinical manufacturing
  • Partner closely with process development scientists to characterize product and process-related variants, guide purification development, and establish relationships between process parameters and product quality
  • Develop, optimize, and perform selected analytical methods in-house, including assays for protein concentration, purity, aggregation, charge variants, identity, binding, and biological activity
  • Lead analytical characterization of critical quality attributes, including:
    • Glycosylation and other post-translational modifications
    • Primary and higher-order structure
    • Purity, fragmentation, and aggregation
    • Charge heterogeneity
    • Target and Fc receptor binding
    • Cell-based potency and effector-function assays, including ADCC
  • Design analytical comparability studies evaluating Neion-produced proteins against reference products and across process changes, scales, and manufacturing sites
  • Select and manage CROs and specialized analytical laboratories, including drafting scopes of work, evaluating technical capabilities, managing timelines and budgets, and overseeing study execution

Requirements

  • 5+ years of industry experience in analytical development or characterization of monoclonal antibodies or closely related biologics
  • Ph.D. in analytical chemistry, biochemistry, biophysics, pharmaceutical sciences, chemical engineering, or a related field; or equivalent industry experience
  • Strong understanding of monoclonal antibody structure, function, degradation pathways, and critical quality attributes
  • Hands-on experience with several core analytical techniques, such as:
    • SEC-HPLC or UPLC
    • Ion-exchange or other charge-variant methods
    • CE-SDS, capillary electrophoresis, or gel-based methods
    • LC-MS-based intact mass, peptide mapping, or glycan analysis
    • ELISA and other binding assays
    • SPR, BLI, or comparable biophysical binding methods
  • Experience developing, optimizing, qualifying, or transferring analytical methods
  • Experience managing CROs or external analytical laboratories, including defining study requirements, reviewing data, and troubleshooting technical issues
  • Familiarity with CMC regulatory expectations and experience with QA processes

Benefits

Compensation: base salary is expected to be $130-170K depending on experience, with additional bonus compensation, equity compensation, and benefits including health insurance, dental insurance, vision insurance, and 401(k).

Apply