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Manager Analytical Development Jobs in New York (NOW HIRING)

Head of Biologics

New York, NY · On-site

$170K - $230K/yr

This person will initially manage a small team of downstream process development and analytical scientists and will play a central role in building Neion Bio's broader protein development ...

Head of Biologics

Manhattan, NY · On-site

$170K - $230K/yr

This person will initially manage a small team of downstream process development and analytical scientists and will play a central role in building Neion Bio's broader protein development ...

The Development Analyst supports the end-to-end development process by driving visibility ... Oversee and manage stone inventory needs for projects; including stone requests, work order ...

Analyst - Development

New York, NY · On-site

$77K - $85K/yr

The Development Analyst supports the end-to-end development process by driving visibility ... Oversee and manage stone inventory needs for projects; including stone requests, work order ...

Analyst - Development

New York, NY · On-site

$77K - $85K/yr

The Development Analyst supports the end-to-end development process by driving visibility ... Oversee and manage stone inventory needs for projects; including stone requests, work order ...

Showing results 21-40

Manager Analytical Development information

See New York salary details

$36.1K

$84.7K

$145.5K

How much do manager analytical development jobs pay per year?

As of Aug 7, 2026, the average yearly pay for manager analytical development in New York is $84,720.00, according to ZipRecruiter salary data. Most workers in this role earn between $64,000.00 and $99,000.00 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.
What are the most commonly searched types of Analytical Development jobs in New York? The most popular types of Analytical Development jobs in New York are:
What are popular job titles related to Manager Analytical Development jobs in New York? For Manager Analytical Development jobs in New York, the most frequently searched job titles are:
What cities in New York are hiring for Manager Analytical Development jobs? Cities in New York with the most Manager Analytical Development job openings:
Infographic showing various Manager Analytical Development job openings in New York as of July 2026, with employment types broken down into 1% As Needed, 79% Full Time, 14% Part Time, 2% Temporary, and 4% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution, with an average salary of $84,720 per year, or $40.7 per hour.

Head of Biologics

Neion Bio

New York, NY • On-site

$170K - $230K/yr

Full-time

Medical, Dental, Vision, Retirement

Re-posted 10 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 an exceptional Head of Biologics Development & CMC to lead the development of therapeutic proteins produced using Neion Bio's egg-based biomanufacturing platform. This person will own Neion Bio's protein development and CMC strategy, spanning downstream process development, analytical development, product characterization, and regulatory CMC.

This is a role for a technically rigorous and highly collaborative leader who can move fluidly between scientific and regulatory strategy and hands-on problem solving. The ideal candidate has deep experience in biologics (and in particular biosimilars) development, can critically evaluate protein quality and process data, and has led cross-functional CMC programs through regulatory interactions. This person will initially manage a small team of downstream process development and analytical scientists and will play a central role in building Neion Bio's broader protein development organization.

Key Responsibilities:

  • Lead Neion Bio's protein development function, including downstream process development, analytical development, product characterization, and CMC strategy
  • Define product-specific critical quality attributes and establish risk-based strategies for evaluating their potential impact on safety, efficacy, pharmacokinetics, immunogenicity, and biological function
  • Lead the design and interpretation of comparative analytical assessment and biosimilarity programs, including reference-product characterization, lot-selection strategy, analytical similarity, and structure-function studies
  • Provide technical oversight of purification-process development
  • Select and manage CROs, CDMOs, consultants, and other external technical partners, ensuring scientific quality, appropriate study design, and timely execution
  • Lead CMC development planning, including program timelines, technical risk assessments, budgets, resource plans, and decision-making frameworks.
  • Serve as the technical CMC lead in interactions with FDA and other regulatory agencies, including preparation for meetings, responses to agency questions, and implementation of regulatory feedback
  • Contribute to portfolio strategy, program selection, development timelines, budgets, hiring, and organizational planning

Requirements

  • Ph.D. in biochemistry, chemical engineering, bioengineering, pharmaceutical sciences, analytical chemistry, or a related field, with 10+ years of relevant industry experience; an M.S. with 13+ years of experience, or a B.S. with 15+ years of experience. 
  • Deep experience in biologics development, with a technical foundation in downstream process development, analytical development, protein characterization, or a closely related field
  • Deep technical knowledge of protein characteristics, especially glycosylation and other post translational modifications 
  • Substantial technical ownership of at least one biologic program through a major late-stage regulatory milestone, such as BLA or MAA submission, approval, process validation, or commercial readiness.
  • Experience managing scientists and leading cross-functional technical teams
  • Experience selecting and managing CROs, CDMOs, analytical laboratories, and other external development partners

Benefits

Compensation: base salary is expected to be $170K-$230K depending on experience, with additional bonus compensation, equity compensation, and benefits including health insurance, dental insurance, vision insurance, and 401(k).