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$89K

$191.4K

$287.5K

How much do all analytical development cmc jobs pay per year?

As of Jul 26, 2026, the average yearly pay for all analytical development cmc in the United States is $191,412.00, according to ZipRecruiter salary data. Most workers in this role earn between $94,000.00 and $249,000.00 per year, depending on experience, location, and employer.

What is the difference between All Analytical Development Cmc vs Analytical Scientist?

AspectAll Analytical Development CmcAnalytical Scientist
CredentialsBachelor's or Master's in Chemistry, Pharmaceutical Sciences, or related fields; relevant certificationsBachelor's or Master's in Chemistry, Pharmaceutical Sciences, or related fields; relevant certifications
Work EnvironmentPharmaceutical or biotech R&D labs, manufacturing supportResearch labs, quality control, or manufacturing settings
Industry UsageUsed in CMC (Chemistry, Manufacturing, and Controls) documentation and developmentCommonly used in analytical testing, method development, and validation

All Analytical Development Cmc professionals focus on developing and validating analytical methods specifically for CMC documentation and regulatory submissions. Analytical Scientists often work on analytical testing and method development across various stages of product development. While both roles require similar educational backgrounds and work environments, All Analytical Development Cmc roles are more specialized in CMC processes, whereas Analytical Scientists may have broader analytical responsibilities.

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What cities are hiring for All Analytical Development Cmc jobs? Cities with the most All Analytical Development Cmc job openings:
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All Analytical Development Cmc jobs near you
Infographic showing various All Analytical Development Cmc job openings in the United States as of July 2026, with employment types broken down into 1% As Needed, 72% Full Time, 23% Part Time, 1% Temporary, and 3% Contract. Highlights an 94% Physical, 1% Hybrid, and 5% Remote job distribution, with an average salary of $191,412 per year, or $92 per hour.

Head of Biologics Development & CMC

Neion Bio

Manhattan, NY • On-site

$170K - $230K/yr

Full-time

Medical, Dental, Vision, Retirement

Posted 18 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 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).

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