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How much do formulation development jobs pay per hour?

As of May 29, 2026, the average hourly pay for formulation 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.

What are the key skills and qualifications needed to thrive in Formulation Development, and why are they important?

To excel in Formulation Development, a solid background in chemistry, pharmaceutical sciences, or related fields, often with a relevant degree, is essential. Experience with analytical instruments, formulation software, and knowledge of Good Manufacturing Practices (GMP) or regulatory guidelines are typically required. Strong problem-solving abilities, attention to detail, and effective cross-functional communication set top performers apart. These skills ensure the creation of safe, effective, and compliant products that meet both scientific and regulatory standards.

What are some common challenges faced in a Formulation Development role, and how are they typically addressed?

Professionals in Formulation Development often encounter challenges such as ensuring product stability, achieving desired drug release profiles, and scaling up formulations from the laboratory to manufacturing. These challenges are typically addressed by conducting thorough pre-formulation studies, collaborating closely with analytical and process engineers, and performing iterative testing to optimize formulations. Teamwork and effective communication with quality assurance and regulatory teams are also crucial to ensure products meet both efficacy and compliance standards.

What is formulation development?

Formulation development is the process of designing and optimizing the composition of a pharmaceutical product, such as a tablet, capsule, or injectable, to ensure its safety, efficacy, and stability. This involves selecting appropriate active ingredients, excipients, and delivery methods to achieve the desired therapeutic effect. Professionals in formulation development work to address challenges like solubility, bioavailability, and manufacturability, while ensuring compliance with regulatory standards. Their work is essential for turning a drug candidate into a viable, market-ready product.

What is the difference between Formulation Development vs Formulation Scientist?

AspectFormulation DevelopmentFormulation Scientist
CredentialsBachelor's or Master's in Pharmacy, Chemistry, or related fieldsBachelor's or Master's in Pharmacy, Chemistry, or related fields
Work EnvironmentResearch labs, pharmaceutical companies, R&D departmentsResearch labs, pharmaceutical companies, R&D departments
Industry UsageDesigning and optimizing drug formulations for productionDeveloping and testing drug formulations, conducting experiments

Formulation Development focuses on designing and optimizing drug formulations for manufacturing, while Formulation Scientists conduct experiments and testing to develop these formulations. Both roles require similar educational backgrounds and work environments, but their specific responsibilities differ in scope and focus.

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Formulation Development jobs near you
Infographic showing various Formulation Development job openings in the United States as of May 2026, with employment types broken down into 4% Internship, 82% Full Time, and 14% Contract. Highlights an 98% In-person, and 2% Remote job distribution, with an average salary of $47,488 per year, or $22.8 per hour.
Associate Director, Formulation and Drug Product Development

Associate Director, Formulation and Drug Product Development

Dyne Therapeutics

Waltham, MA

Other

Posted 25 days ago

Job description

Role Summary:

The Associate Director, Formulation and Drug Product Development will be accountable for all internal and external activities related to successful formulation development for Dyne's bioconjugate drug products to ensure favorable manufacturability, product quality, and long-term stability. This role will partner closely with colleagues in Research, Pharmaceutical Quality, and Manufacturing to define Dyne's strategy for bringing best-in-class medicines to patients in need, including high-concentration formulations for subcutaneous administration and lyophilized drug products to ensure seamless supply of all drug products for clinical trials.

This role is based in Waltham, MA without the possibility of being a remote role. Physical presence onsite is expected on 4-5 days/week.

Primary Responsibilities Include:

  • Act as the subject matter expert for drug product development within the Technical Development group, including formulation development, selection of container closure systems, and sterile fill finish clinical manufacturing.
  • Act as main point of contact for CDMO(s) for external formulation development activities, and liaise with the Research group to define, streamline and execute early-stage formulation development efforts.
  • Build and enhance internal capabilities for formulation development in the laboratory.
  • Responsible for development, tech transfer, and scale-up of drug product processes, and cGMP manufacturing of clinical grade drug product (Phase 1-3).
  • Key contributor to drug product sections of early-stage clinical filings (INDs/IMPDs/Health Canada).
  • Collaborate with Technical Development, Manufacturing, Quality Control, Quality Assurance, and Regulatory Affairs to ensure continuity of drug supply for early clinical evaluation.
  • Responsible for driving execution of the formulation development plan at CDMO (PO through delivery).
  • Champion a strong winning culture, fostering teamwork and commitment to excellence through transparent communication, engagement and collaboration.

Education and Skills Requirements:

  • PhD or equivalent experience in a scientific discipline and a minimum of 8+ years related experience. 
  • Proven experience in clinical drug product formulation development including liquid fill finish, lyophilization, subcutaneous formulations, and other injectables.
  • Expertise in sterile fill-finish early clinical manufacturing as well as understanding of analytical techniques that support manufacturing activities.
  • Demonstrated understanding of the principles and applications associated with external manufacturing operations from development to clinical manufacturing.
  • Strong experience and knowledge of cGMP manufacturing requirements.
  • Strategic thinker with a sense of urgency to deliver quality results on time and in a highly ethical and professional manner.
  • Experience managing complex schedules and priorities in a dynamic biotech environment.
  • Ability to work, influence, and gain consensus across multiple functions (Technical Operations, Quality and Regulatory Affairs).
  • Collaborative work style to be part of a team to identify process gaps and constructively develop solutions.
  • Excellent interpersonal, verbal, and written communication skills with the ability to establish strong cross-functional relationships.
  • Resilient and able to work in a demanding, fast-paced environment and capable of supporting multiple programs and vendors.

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