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Associate Formulation Scientist Jobs in California

Scientist I - III

Fremont, CA · On-site

$80K - $179K/hr

Associate Director, CMC and Bioanalytics PURPOSE OF THE JOBRani Therapeutics has developed a ... Experience in providing support to formulation development and process development. * Aseptic ...

Showing results 21-40

Associate Formulation Scientist information

What are the key skills and qualifications needed to thrive as an associate formulation scientist?

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:
Infographic showing various Associate Formulation Scientist job openings in California as of August 2026, with employment types broken down into 1% As Needed, 69% Full Time, 27% Part Time, 1% Temporary, and 2% Contract. Highlights an 97% Physical, 1% Hybrid, and 2% Remote job distribution.

Scientist II, Downstream Viral Vector Process Development

GeneFab

Alameda, CA • On-site

$130K - $150K/yr

Full-time

Re-posted 14 days ago


Job description

GeneFab is seeking an experienced Downstream Process Development Scientist/Lead focused on viral vector purification (AAV and Lentiviral) for in vivo gene therapy. It is a technical, project-based role within a CRDMO environment that balances hands-on process optimization with cross-functional leadership and client-facing responsibilities.
Responsibilities
  • Design, optimize, and scale-up downstream processes for the purification of viral
    vectors, with a focus on in vivo gene therapy products and lentiviral vectors.
  • Execute experimental plans, analyze data, and provide insightful
    recommendations to improve process efficiency, yield, and product quality.
  • Collaborate with cross-functional teams, including Upstream Process
    Development, Analytical Development, and Manufacturing, to ensure seamless
    integration of processes.
  • Troubleshoot and resolve technical challenges in downstream processes, ensuring
    robust and scalable solutions.
  • Present internally and to client with project status updates
  • Stay abreast of industry trends, emerging technologies, and regulatory guidelines
    to contribute to the continuous improvement of processes and compliance.
  • Provide direction and leadership to development associates as the team expands.

Qualifications
  • Ph.D. or Master's degree in Chemical Engineering, Biochemical Engineering,
    Biotechnology, or related field with a minimum of 3 years (Ph.D.) or 5 years
    (Master's) of relevant industry experience
  • Proven expertise in downstream process development for viral vectors, with a
    focus on AAV and lentiviral vectors.
  • Hands-on experience with chromatography, filtration, TFF and other downstream
    processing techniques.
  • Strong analytical and problem-solving skills, with the ability to interpret complex
    data sets.
  • Excellent communication skills and the ability to work collaboratively in a team
    environment.
  • Knowledge of regulatory requirements and quality standards related to
    biopharmaceutical manufacturing.
  • Experience with formulation science preferred

$130,000 - $150,000 a year
About GeneFab
GeneFab is a contract manufacturing and synthetic biology biofoundry focused on cell and gene therapies. GeneFab was formed in 2023 with a vision to combine industry leading expertise in synthetic biology with advanced cGMP capabilities in order to accelerate the development and commercialization of genetic medicines. GeneFab offers its customers an extensive technology platform and know-how that spans early stage product design, technical development, and cGMP compliant production. GeneFab's technology platform includes bioinformatic-guided discovery of cell type promoters, directed evolution of small molecule-regulated gene switches, and the engineering of highly sensitive kill switches for enhanced safety and control of cellular therapies.
We are committed to an inclusive and diverse GeneFab. We believe that different perspectives lead to better ideas, and better ideas allow us to better understand the needs and interests of our diverse GeneFab team. We welcome people of different backgrounds, experiences, abilities, and perspectives and are an equal opportunity employer.
We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.