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Protein Formulation Scientist Jobs (NOW HIRING)

Glanbia

Senior Beverage Scientist

Valencia, CA · On-site

Strong formulation skills across proteins, carbohydrates, lipids, hydrocolloids, emulsions, sweeteners, acids, minerals, and flavor systems. * Working knowledge of colloid science, protein chemistry ...

Glanbia

Senior Beverage Scientist

Valencia, CA · On-site

Strong formulation skills across proteins, carbohydrates, lipids, hydrocolloids, emulsions, sweeteners, acids, minerals, and flavor systems. * Working knowledge of colloid science, protein chemistry ...

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Protein Formulation Scientist information

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How much do protein formulation scientist jobs pay per hour?

As of Sep 11, 2026, the average hourly pay for protein formulation scientist in the United States is $37.61, according to ZipRecruiter salary data. Most workers in this role earn between $25.24 and $43.51 per hour, depending on experience, location, and employer.

What does a protein formulation scientist do?

A Protein Formulation Scientist specializes in developing and optimizing formulations for protein-based drugs, ensuring their stability, efficacy, and safety for therapeutic use. This role involves selecting appropriate excipients, designing experiments to test formulations, and analyzing data to meet regulatory standards. Protein Formulation Scientists work closely with other scientists and engineers to address challenges such as protein aggregation, degradation, and delivery. They play a vital role in the pharmaceutical and biotechnology industries, contributing to the development of life-saving biologic medications.

What are the key skills and qualifications needed to thrive as a protein formulation scientist?

To thrive as a Protein Formulation Scientist, you need expertise in biochemistry, protein chemistry, and formulation science, typically supported by an advanced degree in a related field. Familiarity with analytical instrumentation (e.g., HPLC, mass spectrometry), formulation software, and regulatory guidelines is essential. Strong problem-solving skills, attention to detail, and effective communication set outstanding scientists apart. These skills are crucial to ensure stable, effective protein products and successful collaboration in multidisciplinary environments.

What are some common challenges faced by protein formulation scientists when developing stable biopharmaceutical products?

Protein Formulation Scientists often encounter challenges such as protein aggregation, degradation, and maintaining bioactivity during formulation development. These issues require careful selection of excipients, optimization of pH, and rigorous stability testing. Additionally, working within cross-functional teams, Protein Formulation Scientists must effectively communicate findings to process development, analytical, and regulatory colleagues to ensure successful product advancement. Staying up-to-date with the latest analytical techniques and regulatory guidelines is also crucial for overcoming these challenges.

What are popular job titles related to Protein Formulation Scientist jobs?

For Protein Formulation Scientist jobs, the most frequently searched job titles are:

Infographic showing various Protein Formulation Scientist job openings in the United States as of August 2026, with employment types broken down into 1% Internship, 1% As Needed, 82% Full Time, 12% Part Time, and 4% Contract. Highlights an 82% Physical, 3% Hybrid, and 15% Remote job distribution, with an average salary of $78,236 per year, or $37.6 per hour.

Senior Scientist, Formulation and DP Development

South San Francisco, CA • On-site

Sutro Biopharma
Biotechnology Research and Development • 51 - 200 employees
Learn more about Sutro Biopharmaexternal

Full-time

Re-posted 5 days ago

Job description

Description
Senior Scientist, Formulation and DP Development
Sutro Biopharma, Inc. is looking for a technical leader who will report to the Executive Director of Formulation and DP Development. You will be developing new compositions for biologic / conjugated molecules and creating robust DP manufacturing processes to advance Sutro pipeline and enhance our internal and collaborative product development initiatives in a fast-paced environment.
Responsibilities:
The candidate we are seeking will work within our Formulation and DP Development team to participate in formulation and DP development for phase appropriate liquid and lyophilized formulations for intermediates, drug substance and drug products. The successful candidate will participate in activities in technology transfer to CMO's. The position is expected to design, execute, document formulation, stability and in-use/compatibility studies to support the final formulation, clinical administration and manufacturing processes. The position will utilize/implement fit-for-purpose analytical methods for biophysical characterization, formulation and process development and stability testing. This position is expected to communicate experimental data both verbally at group, department and cross functional meetings and through written documents and reports that may be included in regulatory filings.
Qualifications:
  • BS/MS (12+ years) or PhD (7+ years) of experience in scientific discipline (Pharmaceutical Sciences, Chemistry, Chemical Engineering, Biomedical Engineering, or related discipline) and demonstrated scientific creativity and contributions
  • Solid technical skills and experience in pre-formulation screening studies, biophysical/ biochemical characterization of proteins, analytical method development and protein/ antibody/ADC product development is essential
  • Practical experience with design and execution of in-use stability studies for biologics and compatibility with administration components
  • Demonstrated ability to design experiments and routinely generate new ideas and original research. High level of scientific initiative and independence. Highly autonomous requiring minimal supervision from manager.
  • Analytical instrumentation such as chromatographic (HPLC, UPLC, column chromatography), visible and subvisible particle analysis, capillary electrophoresis and/or biophysical techniques (UV-vis, MALS/DLS, DSC, CD, FTIR, AUC, Fluorescence spectroscopy) for protein characterization are highly desirable.
  • Able to cooperate effectively with cross functional teams, such as up and down stream process development, manufacturing and quality. Ability to quickly adapt to changes in project direction.
  • Working knowledge of cGMP and relevant drug product development guidelines and regulations
  • Flexibility to work on multiple projects between departments in a fast-paced environment is essential.
  • Excellent oral and written communication skills and being detailed oriented are important attributes.

Sound exciting? Apply today and join our team!
Sutro Biopharma, Inc. encourages all colleagues to be fully vaccinated for COVID-19 prior to the first date of employment.
As an equal opportunity employer, we believe in fostering a culture that is inclusive and values diversity in background and opinions. Sutro Biopharma hires extraordinary individuals into every position in the company and is committed to the diversity of our team. Our company progresses without regard of race, ethnicity, gender, sexual orientation, religious belief, age, disability or citizenship status. We are dedicated to creating a safe environment where our employees can grow and succeed together.
We look forward to hearing from candidates who are interested in exploring opportunities with Sutro! Our People & Culture team/hiring managers are unable to respond and do not accept solicitations from third-party agencies.
The anticipated salary range for fully qualified candidates applying for this role at Sutro Biopharma's California based locations will be $155,000 - $168,000 (not including bonus, equity, and benefits). The final salary offered will be dependent on several factors that include and are not limited to relevant previous experience, job responsibilities and duration of experience, the type and length of experience within the industry and education.
About Sutro Biopharma
Sutro Biopharma, Inc. is advancing a next-generation antibody-drug conjugate (ADC) platform designed to deliver single- and dual-payload ADCs that enable meaningful breakthroughs for patients with cancer. By fully optimizing the antibody, linker, and payload, Sutro's cell-free platform produces ADCs that are engineered to improve drug exposure, reduce side effects, and expand the range of treatable tumor types. With unique capabilities in dual-payload ADCs, Sutro aims to overcome treatment resistance and redefine what's possible in cancer therapy. The Company's pipeline of single- and dual-payload ADCs targets large oncology markets with limited treatment options and significant need for improved therapies.

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