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Associate Director Formulation Oral Solids Jobs

adareps

Senior Formulation Scientist I

Vandalia, OH · On-site

... oral solids, powders for constitution, solutions, and suspensions for clinical trials, ANDA, and ... Use experimental design to rapidly optimize formulation composition and in-process specifications.

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$30.5K

$102.7K

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How much do associate director formulation oral solids jobs pay per year?

As of Sep 9, 2026, the average yearly pay for associate director formulation oral solids in the United States is $102,728.00, according to ZipRecruiter salary data. Most workers in this role earn between $70,000.00 and $141,000.00 per year, depending on experience, location, and employer.

What does an Associate Director Formulation Oral Solids do?

An Associate Director Formulation Oral Solids is responsible for leading teams in the development and optimization of oral solid dosage forms, such as tablets and capsules, in the pharmaceutical industry. They oversee formulation strategies, ensure compliance with regulatory standards, and manage projects from early development through to scale-up and commercial manufacturing. This role also involves collaborating with cross-functional teams, mentoring scientists, and supporting technical problem-solving to ensure product quality and efficiency.

What are the key skills and qualifications needed to thrive as an Associate Director Formulation Oral Solids?

To excel as an Associate Director Formulation Oral Solids, you typically need an advanced degree in pharmaceutical sciences or related fields, along with extensive experience in oral solid dosage form development and team leadership. Familiarity with formulation technologies, regulatory guidelines (such as FDA and ICH), and quality systems, as well as experience with analytical instrumentation and project management tools, is essential. Strong leadership, problem-solving abilities, and effective communication skills distinguish top performers in this role. These competencies are crucial for ensuring robust product development, regulatory compliance, and successful cross-functional collaboration in a highly regulated industry.

What are the typical responsibilities of an Associate Director Formulation Oral Solids in leading project teams?

As an Associate Director Formulation Oral Solids, you will often oversee cross-functional teams responsible for developing and optimizing oral solid dosage forms. Your responsibilities include setting project timelines, coordinating with analytical, manufacturing, and regulatory groups, and ensuring formulation strategies align with both scientific and business objectives. A key challenge is balancing technical problem-solving with effective team leadership and communication across departments to keep projects on track. This leadership role also offers opportunities for mentoring junior scientists and contributing to long-term R&D strategy.

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

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

Infographic showing various Associate Director Formulation Oral Solids job openings in the United States as of September 2026, with employment types broken down into 97% Full Time, and 3% Temporary. Highlights an 94% In-person, and 6% Remote job distribution, with an average salary of $102,728 per year, or $49.4 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 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.
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