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Internship Pharmaceutical Formulation Development Jobs

BioCT Innovation Commons

$90 - $110/hr

Participate in customer formulation development projects (primarily pharmaceutical) and development of new drug delivery technologies as a hands-on laboratory scientist/engineer * Collaborate with ...

Alkermes

Scientist, Formulation Development

Waltham, MA · On-site

$136/hr

S. in Chemical Engineering, Pharmaceutical Sciences, Materials Science, or a related field, with 0 ... controlledrelease) formulation development. * Experience or exposure to Process Analytical ...

Alkermes

Scientist, Formulation Development

Waltham, MA · On-site

$136/hr

Collaborate effectively within Pharmaceutical Development and cross-functional project teams ... formulation development. * Experience or exposure to Process Analytical Technology (PAT), and/or ...

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How much do internship pharmaceutical formulation development jobs pay per hour?

As of Aug 27, 2026, the average hourly pay for internship pharmaceutical formulation development in the United States is $21.19, according to ZipRecruiter salary data. Most workers in this role earn between $17.31 and $24.04 per hour, depending on experience, location, and employer.

What is the difference between Internship Pharmaceutical Formulation Development vs Pharmaceutical Formulation Scientist?

AspectInternship Pharmaceutical Formulation DevelopmentPharmaceutical Formulation Scientist
QualificationsEnrolled in or recent graduate of related degreeBachelor's or Master's in Pharmacy, Chemistry, or related field
Work EnvironmentTraining-focused, entry-level, supervisedResearch and development labs, project-driven
ResponsibilitiesAssisting in formulation tasks, learning protocolsDesigning, developing, and optimizing formulations

Internship Pharmaceutical Formulation Development roles are entry-level, focusing on learning and assisting with formulation tasks under supervision. In contrast, Pharmaceutical Formulation Scientists are experienced professionals responsible for developing and optimizing drug formulations independently. The internship provides foundational exposure, while the scientist role involves advanced expertise and project leadership.

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Internship Pharmaceutical Formulation Development jobs near you
Infographic showing various Internship Pharmaceutical Formulation 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 90% Physical, 3% Hybrid, and 7% Remote job distribution, with an average salary of $44,083 per year, or $21.2 per hour.

Pharmaceutical Formulation Chemist

Temecula, CA • On-site

K2 Staffing
Recruiting and Staffing Services • 11 - 50 employees
Learn more about K2 Staffingexternal

Contractor

Re-posted 13 hours ago

Job description

Summary

Our client is seeking an experienced Formulation Chemist to support the development of lyophilized injectable vials and oral capsule formulations on a project-based (Statement of Work / Per Diem) basis. This role is ideal for a pharmaceutical formulation expert with hands-on experience developing injectable and oral solid-dose products who can independently lead formulation activities from concept through regulatory readiness.

The successful candidate will have expertise in formulation development, excipient selection, lyophilization, stability studies, GMP documentation, and technical writing while collaborating with Quality, Regulatory, Manufacturing, and Analytical teams to support product commercialization.

Duties & Responsibilities Formulation Development
  • Develop formulations for lyophilized injectable vials and oral capsule products.
  • Design and execute formulation development studies, including excipient selection, buffer optimization, and compatibility assessments.
  • Troubleshoot formulation challenges related to solubility, stability, aggregation, dissolution, and product performance.
  • Support scale-up activities from laboratory development through manufacturing.
Lyophilization & Injectable Products
  • Develop and optimize lyophilization cycles, including freezing, primary drying, and secondary drying.
  • Investigate and resolve reconstitution and product stability issues.
  • Support sterile fill-finish activities, ensuring compatibility with filtration systems and filling equipment.
Oral Solid Dose Development
  • Develop oral capsule formulations, including excipient compatibility and fill-weight uniformity.
  • Evaluate formulation performance and identify opportunities to improve bioavailability where appropriate.
  • Generate technical data packages supporting manufacturing partners.
Stability, Documentation & Regulatory Support
  • Design and execute accelerated and long-term stability studies in accordance with ICH guidelines.
  • Prepare formulation development reports, technical protocols, batch records, and supporting GMP documentation.
  • Collaborate with Quality and Regulatory teams to ensure formulation data supports regulatory compliance, including 503A/503B requirements.
  • Support manufacturing and analytical teams by providing formulation expertise throughout the product lifecycle.
Qualifications & Requirements Required Experience
  • Bachelor's or Master's degree in Chemistry, Pharmaceutical Sciences, Chemical Engineering, or a related scientific discipline (PhD preferred).
  • Minimum 3 years of pharmaceutical formulation experience developing both injectable (lyophilized) and oral solid-dose products.
  • Hands-on experience with lyophilization cycle development and freeze-drying equipment.
  • Experience developing oral capsule formulations, including excipient selection and fill-weight optimization.
  • Strong understanding of formulation challenges, including solubility, stability, aggregation, and excipient compatibility.
Technical Skills
  • Experience designing and executing formulation development studies.
  • Knowledge of GMP documentation, batch records, technical protocols, and formulation reports.
  • Familiarity with ICH stability guidelines and stability protocol development.
  • Understanding of USP <795>, USP <797>, and/or 503A/503B regulatory requirements preferred.
  • Experience supporting sterile fill-finish operations and aseptic processing is highly desirable.
Professional Skills
  • Strong technical writing and documentation skills.
  • Excellent analytical, problem-solving, and troubleshooting abilities.
  • Ability to work independently while collaborating with cross-functional teams.
  • Strong organizational skills with the ability to manage multiple project priorities.
Employment Type: Contract Location: Temecula, CA