ZipRecruiter

Log In

1

Associate Director Formulation Development Jobs

Debut Biotech

Director, Formulation Sales

San Diego, CA · On-site +1

$150K - $180K/yr

Director, Formulation Sales Summary Are you passionate about bringing breakthrough, science-backed ... Build and maintain strong relationships with key decision makers across R&D, product development ...

next page

Showing results 1-20

All JobsScience JobsResearch JobsScientist JobsAssociate Director Formulation Development Jobs

Associate Director Formulation Development information

See salary details

$21K

$93.3K

$180K

How much do associate director formulation development jobs pay per year?

As of Sep 9, 2026, the average yearly pay for associate director formulation development in the United States is $93,350.00, according to ZipRecruiter salary data. Most workers in this role earn between $72,500.00 and $103,000.00 per year, depending on experience, location, and employer.

What cities are hiring for Associate Director Formulation Development jobs?

Cities with the most Associate Director Formulation Development job openings:

What states have the most Associate Director Formulation Development jobs?

States with the most job openings for Associate Director Formulation Development jobs include:

What are popular job titles related to Associate Director Formulation Development jobs?

For Associate Director Formulation Development jobs, the most frequently searched job titles are:

Infographic showing various Associate Director Formulation Development job openings in the United States as of June 2026, with employment types broken down into 100% Full Time. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution, with an average salary of $93,350 per year, or $44.9 per hour.

Associate Director, Formulation Development

Burlington, MA • On-site

Scorpion Therapeutics
51 - 200 employees
Learn more about Scorpion Therapeuticsexternal

Other

Posted 8 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.
#J-18808-Ljbffr

Apply