Formulation development jobs

Senior Expert, (Drug Product Development)

Novartis · Posted Nov 13, 2026

Open

Mengeš, Municipality of Mengeš, Slovenia
Hybrid
Full-time · Senior
€47K–€86K per year

Senior Expert, (Drug Product Development)

Novartis · Posted Nov 13, 2026

Open

Mengeš, Municipality of Mengeš, Slovenia
Hybrid
Full-time · Senior
€47K–€86K per year

Senior Scientist, Formulation Development, Oral Drug Product Development

Bristol Myers Squibb · Posted Nov 12, 2026

Open

New Brunswick, New Jersey, United States
Full-time · Senior
$118K–$143K per year
2–9 years

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Senior Scientist responsible for formulation design, development, characterization, and technology transfer of oral drug products.

Compensation

New Brunswick - NJ - US: $118,140 - $143,160

Responsibilities

Collaborate across BMS sites with Drug Product, Analytical, API, Quality, and Regulatory functions to execute drug product formulation/process development
Develop oral formulations for clinical studies and commercialization
Lead drug product formulation and process development including evaluating the need and potential for enhancing oral bioavailability, stability, and processability of drug candidates
Support preparation of CMC regulatory documents
Support departmental initiatives for assigned projects and methodologies

Requirements

BS in Pharmaceutical Science, Chemical Engineering, or related discipline
MS
Ph.D.

Skills

formulation development pharmaceutical processing drug substance excipients

Senior Scientist, Formulation Development, Oral Drug Product Development

Bristol Myers Squibb · Posted Nov 12, 2026

Open

New Brunswick, New Jersey, United States
Full-time · Senior
$118K–$143K per year
7–9 years

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Senior Scientist responsible for formulation design, development, characterization, and technology transfer of oral drug products.

Compensation

New Brunswick - NJ - US: $118,140 - $143,160

Responsibilities

Collaborate across BMS sites to execute drug product formulation/process development
Develop oral formulations for clinical studies and commercialization
Lead drug product formulation and process development
Support preparation of CMC regulatory documents
Support departmental initiatives for assigned projects

Requirements

BS in Pharmaceutical Science, Chemical Engineering, or related discipline
MS with 4-6 years of experience
Ph.D. with 2-4 years of experience

Skills

formulation development pharmaceutical processing blending milling sieving granulation

Scientist, Dissolution & Biopharmaceutical Modeling

Lilly · Posted Nov 11, 2026

Open

Indianapolis, Indiana, United States
Full-time
$66K–$172K per year

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Lead analytical chemistry and biopharmaceutical modeling efforts to support early clinical formulation development and drug product performance for synthetic drug molecules.

Compensation

$66,000 - $171,600

Responsibilities

Develop analytical methods and conduct experiments to aid early clinical formulation development
Collaborate with formulation scientists to design experiments and guide selection and characterization of formulations
Partner with biopharmaceutical modeling scientists, analytical chemists, pharmaceutical scientists, and engineers to identify appropriate drug form, formulation, and process characteristics
Identify and mitigate technical risks for performance and production of clinical and commercial drug products
Operate, maintain, and troubleshoot automated dissolution systems, including hardware and instrument control software

Requirements

B.S. in Chemistry, Biochemistry, Pharmaceutical Science, or other directly related discipline (e.g., Material Science)
Nice to have: career experience relevant to the position
Nice to have: development, validation, and transfer of analytical methods
Nice to have: operating and troubleshooting automated dissolution systems
Nice to have: knowledge of biopharmaceutics and pharmacokinetic principles

Skills

Scientist, Dissolution & Biopharmaceutical Modeling

Eli Lilly and Company · Posted Nov 11, 2026

Open

Indianapolis, Indiana, United States
Full-time
$66K–$172K per year

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Lead analytical chemistry and biopharmaceutical modeling to support drug product development and commercialization.

Compensation

$66,000 - $171,600

Responsibilities

Develop analytical methods and conduct experiments for early clinical formulation
Collaborate with formulation scientists to design experiments and guide selection and characterization of formulations
Partner with biopharmaceutical modeling scientists, analytical chemists, pharmaceutical scientists, and engineers to identify appropriate drug form, formulation, and process characteristics
Identify and mitigate technical risks for performance and production of clinical and commercial drug products
Operate, maintain, and troubleshoot automated dissolution systems, including hardware and instrument control software

Requirements

B.S. in Chemistry, Biochemistry, Pharmaceutical Science, or other directly related discipline (e.g., Material Science)
Nice to have: career experience relevant to the position
Nice to have: development, validation, and transfer of analytical methods
Nice to have: troubleshooting automated dissolution systems
Nice to have: knowledge of biopharmaceutics and pharmacokinetic principles

Skills

analytical chemistry

Associate Director, Global Clinical Supply Chain

IMVT Corporation · Posted Nov 10, 2026

Open

Remote, United States
Remote
Full-time · Director
$170K–$200K per year
5+ years

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The Associate Director of Global Clinical Supply Chain is responsible for the successful execution of supply chain management for clinical trials, providing triage support for rapid start-up of CDMOs and CROs, and ensuring continuous supply of Investigational Medicinal Product (IMP).

Compensation

Salary range for posting: $170,000—$200,000 USD

Responsibilities

Managing and executing overall Project Delivery through coordination of CMC efforts assigned to the entire project team (CMC, Supply Chain, Legal, Procurement, Regulatory, Clinical Development, and Clinical Operations).
Provides recommendations on packaging design, distribution and blinding strategy.
Plans and manages execution of initial supplies and resupplies for assigned studies.
Designs and implements plans to supply study drug to complex global clinical trials using sound supply chain techniques.
Develops and executes inventory management plans for clinical sites and depots to ensure treatment availability for every patient visit.

Requirements

Bachelor's degree in science, engineering, or another relevant field
Nice to have: advanced degree

Skills

Clinical supply management CMC regulatory terminology

Scientist - Dove Deodorants

Unilever · Posted Nov 9, 2026

Open

Trumbull, Connecticut, United States
Full-time · Associate
$71K–$81K per year

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Lead formulation development and testing for Dove Deodorants, integrating new technologies into the innovation pipeline and collaborating with cross-functional teams.

Compensation

Pay: The pay range for this position is $71,400 to $81,000. Unilever takes into consideration a wide range of factors that are utilized in making compensation decisions including, but not limited to, skill sets, experience and training, licensure and certifications, qualifications and education, and other business and organizational needs. Bonus: This position is bonus eligible. Long-Term Incentive (LTI): This position is LTI eligible.

Responsibilities

Own formulation, stability, safety and performance testing, processing, specifications and regulatory, compliance and patents
Deliver products against technical briefs, ensuring Formulation, Process, Packaging and Quality Assurance specifications are correct and on time
Work with internal R&D teams to translate technology roadmaps into insightful innovations
Build productive relationships with partners including Process Engineering, Packaging, CTI & Claims, Specifications, Safety, Brand Teams, Supply Chain, 3P manufacturers and RM suppliers
Ensure products deliver a delightful, top-quality consumer experience

Requirements

Bachelor's of Science (BS) degree required; Chemical Engineering or Chemistry preferred
Nice to have: Strong, proven technology and/or project deliveries to market
Nice to have: Hands-on laboratory scale-up activities
Nice to have: Fundamental understanding of deodorant category formulation and processing principles

Principal Scientist, Formulation & Drug Product Development

Denali Therapeutics · Posted Sep 10, 2026

Open

South San Francisco, California, United States
On-site
Full-time · Principal
$159K–$207K per year
10+ years

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Serve as a formulation and drug product process development lead for a growing portfolio of protein biologics, providing technical formulation and drug product expertise across the development lifecycle.

Compensation

Salary Range: $159,000.00 to $207,000.00 . Compensation for the role will depend on a number of factors, including a candidate’s qualifications, skills, competencies, and experience.

Responsibilities

Independently drive formulation and drug product development activities for large molecule biotherapeutics
Design and execute formulation development studies to identify clinical and commercial formulation & dosage form, establish shelf life of DS & DP, assess in-use compatibility, and support comparability assessments
Develop stress comparability strategies to support process changes and scale-up
Oversee drug product process development activities as well as DP process characterization and process validation activities to support clinical and commercial manufacturing
Perform biophysical and biochemical characterization of protein therapeutics in the laboratory using chromatography-, capillary-, spectroscopy-based analytical methods

Requirements

PhD in Chemical Engineering
PhD in Pharmaceutical Sciences
PhD in Biophysics
PhD in Analytical Chemistry
BS or MS with commensurately greater directly relevant experience

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