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Associate Scientist Analytical Development Jobs in Paterson, NJ

Neion Bio

Scientist, Analytical Development

New York, NY · On-site

$130/hr

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 ...

Neion Bio

Scientist, Analytical Development

Manhattan, NY · On-site

$150 - $200/hr

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 ...

IMCD Group

Associate Scientist

Allendale, NJ · On-site

... analytical testing, and laboratorymanagement activities. Working closely with the Senior Scientist ... Supports formulation development projects for oral solid, liquid, topical, and nutraceutical ...

David Protein

Associate Scientist, Quality

New York, NY · On-site

$90K - $110K/yr

The Associate Scientist, Quality is a hands-on, lab-based role responsible for executing quality ... Epogee's R&D and quality functions. This person supports analytical/synthesis procedures ...

IMCD Group

Associate Scientist

Allendale, NJ

... analytical testing, and laboratorymanagement activities. Working closely with the Senior Scientist ... Supports formulation development projects for oral solid, liquid, topical, and nutraceutical ...

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All JobsAssociate Scientist Analytical Development JobsAssociate Scientist Analytical Development Jobs in Paterson, NJ

Associate Scientist Analytical Development information

See Paterson, NJ salary details

$19

$36

$58

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

As of Sep 7, 2026, the average hourly pay for associate scientist analytical development in Paterson, NJ is $36.56, according to ZipRecruiter salary data. Most workers in this role earn between $28.37 and $41.59 per hour, depending on experience, location, and employer.

What does an associate scientist analytical development do?

An Associate Scientist in Analytical Development is responsible for designing, conducting, and analyzing experiments to develop and validate analytical methods used in the testing of pharmaceutical products. They work closely with cross-functional teams to ensure the quality and consistency of drug formulations by using various laboratory techniques such as chromatography, spectroscopy, and wet chemistry. Their role is critical in supporting drug development, regulatory submissions, and ensuring products meet industry standards.

What are some common challenges an associate scientist analytical development might face when working on new drug formulations?

Associate Scientists in Analytical Development frequently encounter challenges such as developing robust analytical methods for complex or novel drug formulations and ensuring these methods meet regulatory standards. Balancing tight project timelines with the need to thoroughly validate methods can also be demanding. Additionally, they often need to troubleshoot unexpected results and collaborate closely with cross-functional teams—including formulation scientists and quality assurance—to resolve technical issues and deliver reliable data. These challenges require strong problem-solving skills and adaptability.

What are the key skills and qualifications needed to thrive as an associate scientist analytical development, and why are they important?

To thrive as an Associate Scientist Analytical Development, you need a solid background in chemistry, biochemistry, or a related field, often supported by a bachelor’s or master’s degree. Familiarity with analytical techniques like HPLC, GC, mass spectrometry, and relevant laboratory information management systems (LIMS) is typically required. Strong problem-solving skills, attention to detail, and effective teamwork are important soft skills for this role. These competencies ensure accurate data generation, regulatory compliance, and successful collaboration in the development of pharmaceutical products.

What is the difference between Associate Scientist Analytical Development vs Associate Scientist Quality Control?

AspectAssociate Scientist Analytical DevelopmentAssociate Scientist Quality Control
Required CredentialsBachelor's or Master's in Chemistry, Biology, or related field; relevant laboratory experienceBachelor's or Master's in Chemistry, Biology, or related field; laboratory experience often focused on testing
Work EnvironmentResearch and development labs, method development, process optimizationQuality control labs, testing, sample analysis, compliance with regulations
Employer & Industry UsagePharmaceutical, biotech companies, focus on method developmentPharmaceutical, biotech companies, focus on product testing and quality assurance

Associate Scientist Analytical Development primarily focuses on developing and optimizing analytical methods for new or existing products, while Associate Scientist Quality Control concentrates on testing and ensuring the quality of products before release. Both roles require similar educational backgrounds but differ in daily tasks and focus areas within the industry.

What are popular job titles related to Associate Scientist Analytical Development jobs in Paterson, NJ?

For Associate Scientist Analytical Development jobs in Paterson, NJ, the most frequently searched job titles are:

Associate Scientist Analytical Development jobs near you
Infographic showing various Associate Scientist Analytical Development job openings in Paterson, NJ as of August 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 100% In-person job distribution, with an average salary of $76,035 per year, or $36.6 per hour.

Scientist, Analytical Development

Neion Bio

New York, NY • On-site

$130/hr

Full-time

Medical, Dental, Vision, Retirement

Re-posted 2 days 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).

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