Senior Principal Scientist

Pfizer

Confirmed live yesterday High trust

Quick summary

Work type
On-site
Location
Pearl River, NY
Salary
$124,400–$207,400 / yr
Posted
2 days ago
Freshness
Confirmed live yesterday
Closes
Sep 29, 2026

Market check

Salary context

Competitive pay

How this pay compares to similar roles

Similar $189k
This role $166k
$112k most similar roles pay here $237k

This role pays less than 60% of similar roles. Most pay $159,000–$218,875 — the shaded band above. At the midpoint, this role pays about $166k versus about $189k for comparable roles.

Based on 240 similar postings.

Employer

About Pfizer

Pfizer Inc. is one of the world''s largest biopharmaceutical companies, researching, developing, manufacturing, and marketing medicines and vaccines across multiple therapeutic areas including oncology, cardiology, and infectious diseases. Industry: Biopharmaceuticals

Pfizer currently has 30 open roles on FindRole.

Listed pay typically runs $115,200–$192,000 across 30 roles with salary data.

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View all roles at Pfizer

At a glance

TL;DR · Senior Principal Scientist

The Senior Principal Scientist joins the Vaccines Research and Development Early Bioprocess Analytical and Formulation Development group as a laboratory-based scientific leader. This role involves defining analytical strategies for early-phase vaccine candidates and adjuvant products, including proteins, mRNAs, conjugates, or combination modalities. The individual will manage a team of scientists, providing coaching and performance support while overseeing the development, qualification, and lifecycle management of separation-based, spectroscopic, mass spectrometry, and other physicochemical analytical methods. Key responsibilities include resolving complex technical challenges, leading cross-functional initiatives, and driving innovation in AI, automation, and digital tools to improve data quality. The candidate must possess expertise in liquid chromatography, capillary electrophoresis, and multivariate data analysis to solve problems related to product quality attributes and ensure robust development of vaccine candidates through high-impact technical recommendations and comprehensive documentation.

What does a Scientist earn?

Median $150600 from 31 postings across 9 companies.

See salary data

What you'll do

  • Define and lead analytical control strategies for multiple vaccine programs based on product quality attributes and risk profiles.
  • Manage a team of scientists by providing direction, prioritization, coaching, and performance support.
  • Lead the development, optimization, qualification, and lifecycle management of separation-based, spectroscopic, and mass spectrometry methods.
  • Resolve complex and ambiguous analytical challenges using mechanistic understanding, experimental design, and cross-disciplinary input.
  • Represent Analytical Development on cross-functional teams to communicate risks and data-driven recommendations to leadership.
  • Drive innovation in analytical technologies, including AI, automation, and digital tools to improve throughput and decision quality.
  • Direct the authoring and technical review of analytical methods, protocols, reports, and regulatory content.
  • Forecast resource needs and coordinate matrixed contributions to ensure high-quality data delivery under strict quality standards.

What we're looking for

  • PhD with at least 8 years of experience in analytical chemistry, biochemistry, pharmaceutical sciences, or a related discipline.
  • Advanced expertise in analytical method development and characterization of biologics, vaccines, or complex modalities.
  • Demonstrated experience managing and leading scientific teams through coaching, prioritization, and professional guidance.
  • Extensive hands-on leadership experience with separation-based techniques such as liquid chromatography or capillary electrophoresis.
  • Proven ability to lead method development, qualification, transfer, and technical documentation across multiple programs.
  • Strong skills in scientific writing, data interpretation, project prioritization, and stakeholder management.
  • Must have permanent work authorization to be employed in the United States.
  • Knowledge of critical quality attributes for mRNA or protein products; experience with LC-MS or automation (preferred).

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