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Pharmaceutical Formulation Development Jobs (NOW HIRING)

TekSky

Hot-melt Extrusion Specialist

Buffalo, NY · On-site

Knowledge of pharmaceutical formulation development * Excellent documentation and analytics skills, including SOPs and batch records * Excellent project management skills * Ability to work in a team ...

Astrix Inc

R&D Formulation Scientist

Columbus, IN · On-site

$27 - $30/hr

... development, formulation science, technical operations, packaging expertise, and in-house ... Bachelor's degree in Microbiology, Biology, Chemistry, Pharmaceutical Sciences, or a related ...

Celcuity Inc.

$150 - $200/hr

The Sr./Principal Scientist role will join a collaborative Pharmaceutical Development group focused on advancing Celcuity's lead drug candidates. The Sr./Principal Scientist will lead formulation and ...

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How much do pharmaceutical formulation development jobs pay per hour?

As of Sep 8, 2026, the average hourly pay for pharmaceutical formulation development in the United States is $50.89, according to ZipRecruiter salary data. Most workers in this role earn between $34.62 and $81.49 per hour, depending on experience, location, and employer.

What is pharmaceutical formulation development?

A Pharmaceutical Formulation Development job involves designing and optimizing drug formulations to ensure safety, efficacy, and stability. Professionals in this role work on selecting appropriate excipients, determining dosage forms, and improving drug delivery methods. They collaborate with regulatory teams to meet compliance standards and conduct tests to assess product performance. This role is essential for bringing new medications from the research phase to commercial production.

What are the main responsibilities of someone working in pharmaceutical formulation development?

Professionals in Pharmaceutical Formulation Development are typically responsible for designing and optimizing drug formulations, conducting laboratory experiments, and ensuring products meet safety, efficacy, and stability standards. Their work often involves collaborating closely with analytical, manufacturing, and regulatory teams to advance products from early development to commercial scale-up. They may also troubleshoot formulation issues, document experimental results, and contribute to regulatory submissions. The role requires careful attention to detail, a strong scientific foundation, and the ability to work both independently and as part of a multidisciplinary team.

What are the key skills and qualifications needed to thrive in pharmaceutical formulation development?

To thrive in Pharmaceutical Formulation Development, you generally need a strong background in pharmaceutical sciences, chemistry, or related fields, and experience with drug formulation principles and analytical techniques. Familiarity with laboratory instrumentation (such as HPLC, dissolution testers), regulatory documentation systems, and GMP/GLP compliance is essential. Excellent problem-solving abilities, attention to detail, and cross-functional communication skills help you excel in a team-oriented environment. These competencies ensure the creation of safe, effective, and commercially viable pharmaceutical products that meet regulatory standards.

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Pharmaceutical Formulation Development jobs near you
Infographic showing various Pharmaceutical Formulation Development job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 82% Full Time, 14% Part Time, and 2% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution, with an average salary of $105,849 per year, or $50.9 per hour.

Director, Formulation Development

Acadia Pharmaceuticals Inc.

Princeton, NJ • Hybrid

Full-time

Re-posted 23 days ago

Job description

Please note that this position can be based in Princeton, NJ. Acadia's hybrid model requires this role to work in our office three days per week on average.Position Summary

The Director, Formulation Development leads formulation, primary packaging, and manufacturing process development across Acadia's portfolio of drug candidates from early development through commercialization. This role provides technical leadership for externalized drug product development across oral solid, liquid, and injectable dosage forms, with a primary focus on oral solid dosage forms. The position is responsible for managing Contract Service Providers (CSPs), resolving complex technical issues, and advancing manufacturing process technologies that support clinical supply, process validation, and lifecycle management. This role plays a key part in reducing development risk, improving execution, and accelerating program progression.

Primary Responsibilities
  • Design and develop pharmaceutical formulations and manufacturing processes to support clinical development, registration, and product launch
  • Evaluate and qualify Contract Service Providers (CSPs) to support development, scale-up, and commercialization, and manage related supplier agreements as needed
  • Lead and oversee the development and scale-up of clinical formulations and finished dosage forms at CSPs, serving as on-site technical support when required
  • Plan and direct scientific and technical activities, including data interpretation, evaluation of results, development of conclusions, and preparation of technical reports and presentations
  • Partner with clinical supply management to define supply requirements and align CSP manufacturing schedules to ensure uninterrupted availability of clinical trial materials
  • Conduct risk assessments of manufacturing processes and products at key development milestones and drive resolution of findings with relevant CSPs
  • Author and review technical reports and development documentation to support regulatory submissions, including review of MBRs, BPRs, and CSP-generated reports
  • Collaborate with analytical, manufacturing, quality, and regulatory teams to develop plans and protocols for drug product development and lifecycle management
  • Ensure compliance with cGMP and applicable GxP requirements, and support CSP readiness for health authority and pre-approval inspections
  • Perform other responsibilities as assigned
Education, Experience, and Skills
  • Advanced degree in Pharmaceutical Sciences, Chemistry, Chemical Engineering, Materials Science, or a related field required; an equivalent combination of education and relevant industry experience may be considered. Minimum of 10 years of progressively responsible experience in formulation and manufacturing process development, including leadership responsibilities. Proven success in formulation and dosage form development, with experience authoring technical reports and CMC sections for regulatory submissions.
  • Deep understanding of dosage form formulation, primary packaging, manufacturing process development, scale-up, optimization, and validation
  • Demonstrated success in oral solid dosage form development of new chemical entities
  • Strong knowledge of cGMP requirements and experience supporting regulatory filings, including NDAs or other marketing authorization applications
  • Proven ability to manage external development and manufacturing partners, including CROs, CMOs, and CSPs
  • Strong written and verbal communication skills, with the ability to translate complex technical information for cross-functional audiences
  • Demonstrated leadership, influence, and resource alignment across functions to achieve development and organizational goals
  • Flexibility to travel domestically and internationally
Physical Requirements

While performing the duties of this job, the employee is regularly required to stand, walk, sit, use hands to handle or feel objects, reach with hands and arms, climb or balance, stoop, kneel, crouch, and see, speak, or hear in a standard office environment and independently from remote locations. The employee must occasionally lift and/or move up to 20 pounds. Ability to travel domestically and internationally is required.

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