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Formulation Analytical Development Jobs (NOW HIRING)

BridgeBio Pharma

Director, Analytical Development

Responsibilities Support Analytical (CMC) activities associated with the formulation of infigratinib. Work closely with your Analytical Development colleagues and external CROs/CMOs collaborators to ...

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As of Sep 8, 2026, the average hourly pay for formulation analytical development in the United States is $22.83, according to ZipRecruiter salary data. Most workers in this role earn between $18.27 and $22.84 per hour, depending on experience, location, and employer.

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Infographic showing various Formulation Analytical Development job openings in the United States as of August 2026, with employment types broken down into 1% As Needed, 83% Full Time, 14% Part Time, and 2% Contract. Highlights an 86% Physical, 3% Hybrid, and 11% Remote job distribution, with an average salary of $47,488 per year, or $22.8 per hour.

Associate Director, Formulation Development

Burlington, MA • On-site

Scorpion Therapeutics
51 - 200 employees
Learn more about Scorpion Therapeuticsexternal

$200 - $250/hr

Other

Posted 7 days ago

Job description

Associate Director, Formulation DevelopmentKey Responsibilities
  • Lead and contribute to the design, development, and optimization of pharmaceutical formulations for peptide therapeutics.
  • Oversee formulation development laboratory activities.
  • Support implementation of analytical methods for characterizing peptides, including chromatographic, spectroscopic, and physical characterization.
  • Oversee and ensure robust QC procedures and compliance with regulatory guidance and industry standards (e.g., ICH guidelines).
  • Plan and conduct non-GMP stability studies; contribute to GMP stability study design to assess shelf-life and degradation pathways.
  • Lead and contribute to drug product process optimization studies to enhance performance and manufacturability at scale; contribute to process transfer to CDMOs.
  • Identify and address formulation and analytical technical challenges (e.g., design experiments, root cause analyses).
  • Partner with Regulatory personnel to incorporate formulation/analytical data into regulatory documents.
Education & Qualifications (Required/Preferred)
  • BS/MS/PhD in pharmaceutical sciences, analytical chemistry, biochemistry, or related field; 8+ years relevant industrial experience emphasizing formulation and analytical development.
  • In-depth understanding of peptide physicochemical stability and experience optimizing parenteral (liquid and lyophilized) formulations.
  • Combination products/devices experience highly desirable.
  • Hands-on analytical methods experience (SEC, RP-HPLC, LC-MS, subvisible particle analysis).
  • Experience in lyophilization formulation, cycle development, and analytical testing.
  • Familiarity with end-to-end CMC drug development, critical milestones, and bottlenecks.
  • CMC regulatory knowledge for parenteral drugs (e.g., FDA, EMA).
  • Strong self-starter, analytical/problem-solving skills, communication, and organizational/multitasking ability in a fast-paced environment.
Travel
  • Periodic travel as needed by the business, including attendance at Together Weeks, Together Days, and functional meetings.
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