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Manager Analytical Development Jobs (NOW HIRING)

Neion Bio

Scientist, Analytical Development

New York, NY · On-site

$130/hr

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 ...

Granules

Manager, Analytical R&D

Chantilly, VA · On-site

$100K - $130K/yr

Work closely with Product development team to manage and coordinate analytical activities on development samples. * Plan and design of experiments toward answering CMC deficiencies responses. * Work ...

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How much do manager analytical development jobs pay per year?

As of Aug 13, 2026, the average yearly pay for manager analytical development in the United States is $77,438.00, according to ZipRecruiter salary data. Most workers in this role earn between $58,500.00 and $90,500.00 per year, depending on experience, location, and employer.

What are the typical day-to-day responsibilities for a manager analytical development?

As a Manager Analytical Development, your typical day involves overseeing laboratory teams, managing analytical method development and validation projects, and ensuring compliance with relevant quality standards. You’ll often collaborate with R&D, quality assurance, and production departments to support product development timelines and troubleshoot analytical challenges. Additionally, you may conduct data reviews, prepare regulatory documentation, and participate in meetings to drive project progress. Your role also includes mentoring team members and optimizing lab workflows for productivity and accuracy.

What is a manager analytical development?

A Manager Analytical Development oversees the development, validation, and implementation of analytical methods to support product development and manufacturing. They ensure compliance with regulatory standards, manage a team of scientists, and collaborate with cross-functional departments to drive innovation and efficiency. Their role is critical in ensuring product quality, consistency, and regulatory approval.

What are the key skills and qualifications needed to thrive in the manager analytical development position, and why are they important?

To excel as a Manager Analytical Development, you typically need an advanced degree in chemistry, biochemistry, or a related field, along with experience in analytical method development and leadership. Familiarity with laboratory information management systems (LIMS), chromatographic software (HPLC/UPLC), and regulatory standards such as ICH and FDA guidelines is common. Outstanding project management, team leadership, and communication skills help you effectively coordinate cross-functional projects and mentor staff. These competencies enable delivery of high-quality analytical solutions, ensure regulatory compliance, and drive successful product development.

What does a Manager Analytical Development do?

A Manager of Analytical Development oversees the design, validation, and implementation of analytical methods used to test and ensure the quality of pharmaceutical or biotech products. They lead teams of scientists, coordinate method development projects, and ensure compliance with regulatory standards such as GMP and FDA guidelines. The role often requires expertise in analytical techniques, laboratory management, and relevant certifications.
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Manager Analytical Development jobs near you
Infographic showing various Manager Analytical Development job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 82% Full Time, 14% Part Time, and 3% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $77,438 per year, or $37.2 per hour.

Scientist, Analytical Development

Neion Bio

New York, NY • On-site

$130/hr

Full-time

Medical, Dental, Vision, Retirement

Re-posted 5 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).