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Associate Formulation Scientist Jobs in California

Gilead

Associate Scientist, FPD

Foster City, CA

$109K - $141K/yr

Small Molecule Formulation and Process Development (FPD) provide formulation, process, and ... An Associate Scientist within FPD may support teams conducting compounding screening to enable drug ...

Gilead

Sr Associate Scientist, FPD

Foster City, CA

$126K - $164K/yr

Small Molecule Formulation and Process Development (FPD) provide formulation, process, and ... A Sr. Associate Scientist within FPD may support teams conducting compounding screening to enable ...

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Associate Formulation Scientist information

What are the key skills and qualifications needed to thrive as an Associate Formulation Scientist, and why are they important?

To thrive as an Associate Formulation Scientist, you need a solid background in chemistry, pharmaceutical sciences, or a related field, often supported by a bachelor's or master's degree. Experience with laboratory techniques, analytical instruments (like HPLC, GC), and familiarity with GLP/GMP regulations are essential. Attention to detail, problem-solving abilities, and effective teamwork are standout soft skills for this role. These skills ensure accurate formulation development, compliance with regulatory standards, and successful collaboration in a research-driven environment.

What is the difference between Associate Formulation Scientist vs Formulation Scientist?

AspectAssociate Formulation ScientistFormulation Scientist
Required CredentialsBachelor's degree in pharmacy, chemistry, or related field; some roles may require 1-2 years of experienceBachelor's or master's degree; typically 2+ years of experience in formulation development
Work EnvironmentLaboratory setting, supporting formulation projects under supervisionLaboratory and development environment, leading formulation tasks
Employer & Industry UsagePharmaceutical, biotech, and cosmetic companiesPharmaceutical and biotech industries, R&D departments

The Associate Formulation Scientist role is an entry-level position supporting formulation development, often with less experience required. The Formulation Scientist typically has more experience and takes on greater responsibility in developing and optimizing formulations. Both roles are common in pharmaceutical and biotech industries, with the Associate position serving as a stepping stone to more advanced formulation roles.

What does an Associate Formulation Scientist do?

An Associate Formulation Scientist is responsible for developing and optimizing formulas for products such as pharmaceuticals, cosmetics, or food items. They conduct experiments to test the stability, safety, and effectiveness of different formulations, often working under the guidance of more senior scientists. Their duties may also include documenting results, preparing reports, and collaborating with other teams such as quality control or production. This role is essential for ensuring that products meet regulatory standards and perform as intended.

What are the typical collaboration points between an Associate Formulation Scientist and other departments?

As an Associate Formulation Scientist, you’ll frequently collaborate with teams from analytical chemistry, quality assurance, regulatory affairs, and manufacturing. This cross-functional interaction is essential for troubleshooting formulation issues, ensuring regulatory compliance, and scaling up laboratory formulations for production. Regular meetings and project updates with these departments not only help streamline workflow but also provide valuable exposure to different areas of the product development process, fostering both learning and career growth.
What are the most commonly searched types of Formulation Scientist jobs in California? The most popular types of Formulation Scientist jobs in California are:
What cities in California are hiring for Associate Formulation Scientist jobs? Cities in California with the most Associate Formulation Scientist job openings:
Associate Formulation Scientist jobs near you
Infographic showing various Associate Formulation Scientist job openings in California as of June 2026, with employment types broken down into 98% Full Time, and 2% Contract. Highlights an 91% Physical, 3% Hybrid, and 6% Remote job distribution.
Associate Scientist Peptide Formulation - Contract

Associate Scientist Peptide Formulation - Contract

Protagonist Therapeutics Inc.

Newark, CA • On-site

$110K - $120K/yr

Full-time

Posted 8 days ago

Job description

Scientist/Associate Scientist Peptide Formulation
Job Description
Protagonist Therapeutics located in Newark, CA is seeking a formulation scientist to support their clinical programs. This person would ideally have experience in design and development of early stage clinical formulations and process development for different delivery routes, particularly oral and parenteral formulation, as well as experience in pre-formulation. Relevant experience could be related to biologics or small molecule, with peptide experience preferred. The ideal candidate would be able to provide formulation expertise and guidance to enable developing clinical formulations for early stage clinical trials. They should be able to design and execute experiments independently in the lab and collaboratively work across all departments involved in clinical development in addition to having a good working knowledge of formulation preparation for preclinical studies.
  • The qualified candidate will be responsible for solid oral dosage form development for early and late-stage clinical trials
  • Should have experience and/or knowledge in pre-formulation, formulation development, and process selection and scale up, oversight of GMP drug product manufacturing and global regulatory CMC (INDs, IMPDs, NDAs) requirements
  • The qualified candidate will be responsible for pre-formulation, formulation development, manufacture of clinical supplies and development of efficient and scalable manufacturing processes.

Required Skills
  • Experienced in formulation and process development of solid oral dosage forms.
  • Expertise in site specific gastrointestinal drug delivery is a plus
  • Hands on experience with modern delivery technologies to enhance bioavailability of small molecule or peptides
  • Knowledge of basic analytical skills required: HPLC/MS, UV, DSC, TGA, XRPD, FTIR, DLS etc.
  • Knowledge in pharmacokinetic data generation and interpretation
  • Excellent communication skills and interpersonal skills are required.

Essential Functions
  • Works under supervision of directors to advance the development of state-of-the-art drug delivery techniques.
  • Represents pharmaceutical sciences in cross-functional team meetings. Presents results of work, interprets data, and draws conclusions regarding presented material and nature of work.
  • Applies formulation development principles and techniques to products and problems. Working under general supervision, plans designs, implements and analyzes laboratory experimentation to advance scientific knowledge of drug formulations.
  • Maintains full working knowledge of principles and theories, applying such knowledge to the direction that supports company interests.
  • Demonstrates emerging ability in developing methods, techniques and evaluation criteria for obtaining results and interpreting experimental outcomes.
  • Thinks critically and creatively and can work independently, determine appropriate resources for resolution of problems and have strong organizational and planning skills.
  • Ability to coordinate with internal and external quality control, quality assurance, and regulatory personnel to resolve technical issues or procedural deviations
  • This is a predominantly lab based position with possibility of international or domestic travel for manufacturing oversight at CDMOs
  • Determine the optimal formulations for discovery compounds based on the delivery route, concentration requirements, and compatibility
  • Provide feedback to chemistry and biology teams to integrate formulation early into the discovery process
  • Experience with formulation laboratory techniques, such as sterile technique, pH, dissolution, lyophilization, spray drying
  • Oversight of formulation screening studies in preclinical animal models
  • Develop a formulation appropriate for Phase 1 clinical studies
  • Generate and interpret pre-formulation data, such as logP, thermal analysis, moisture content, particle size, stability etc.

Experience And Skills
  • 8+ years of experience in peptide or small molecule development with BS in chemistry, engineering, pharmaceutics, or other related scientific discipline (or) 5-8 years with MS in chemistry, engineering, pharmaceutics, or other related scientific discipline (or) 3-5 years of experience in drug formulation with PhD in chemistry, engineering, pharmaceutics, or other related scientific discipline.
  • Demonstrates excellent writing and communication skills

The base pay range for this position at commencement of employment is expected to be between $110K and $120K / year; however, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience.
Protagonist Therapeutics is a discovery through late-stage development biopharmaceutical company. The Company's proprietary peptide technology platform enables de novo discovery of peptide therapeutics. Two novel peptides derived from Protagonist's proprietary discovery platform are at or near commercialization. ICOTYDE™ (icotrokinra) is approved in the U.S. for the treatment of moderate-to-severe plaque psoriasis in adults and pediatric patients 12 years of age and older who weigh at least 40 kg who are candidates for systemic therapy or phototherapy. ICOTYDE is the first and only targeted oral peptide that precisely blocks the Interleukin-23 receptor (IL-23R) licensed to Janssen Biotech, Inc.,a Johnson & Johnson company. ICOTYDE was jointly discovered by Protagonist and Johnson & Johnson scientists, with Protagonist having primary responsibility for the development of ICOTYDE through Phase 1, and Johnson & Johnson assuming responsibility for further development and commercialization. An NDA for rusfertide, a first-in-class hepcidin mimetic peptide that is being co-developed with Takeda Pharmaceuticals pursuant to a worldwide license and collaboration agreement entered in 2024, is under priority review with the FDA. Protagonist holds an option to co-commercialize rusfertide in the U.S. through a 50/50 profit and loss share structure or can opt-out of this structure. The Company also has a number of preclinical stage drug discovery programs addressing clinically and commercially validated targets including an oral IL-17 peptide antagonist, obesity dual and triple agonists, an oral hepcidin functional mimetic, and the recently announced IL-4 and amylin programs.
More information on Protagonist, its pipeline drug candidates, and clinical studies can be found on the Company's website at https://www.protagonist-inc.com.

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