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Research Associate Formulation Development Jobs

Medasource

R&D Formulation Scientist

Summit, NJ · On-site

$25 - $32/hr

Job Title: R&D Formulation Scientist Hourly/Salary Compensation Range: $25-32/hour Contract Length: 8 Months, with strong likelihoods of extension Location: Summit, NJ Hours: 8am-5pm Start Date: ASAP ...

Astrix Inc

R&D Formulation Scientist

Columbus, IN · On-site

$27 - $30/hr

Summary We are seeking an experienced and detail-oriented Senior Microbiologist / Formulation Scientist to join our Research & Development team. The ideal candidate will have 3-5+ years of industry ...

Meridabio

Scientist, Formulation Development

Cambridge, MA · On-site

$125 - $150/hr

Reporting to DP and Formulation group , this individual will contribute to the design, development, characterization, and optimization of formulations for biologic drug candidates from early research ...

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Research Associate Formulation Development information

What does a research associate formulation development do?

A Research Associate in Formulation Development is responsible for designing, developing, and optimizing pharmaceutical formulations, such as tablets, capsules, or injectables. They conduct experiments to evaluate the stability, efficacy, and quality of drug products, often working in a laboratory setting. Their work involves collaborating with scientists, documenting results, and ensuring compliance with regulatory standards. This role is crucial for bringing new medications from the concept stage to clinical trials and eventual market approval.

What are the key skills and qualifications needed to thrive as a research associate formulation development?

To thrive as a Research Associate in Formulation Development, you need a background in pharmaceutical sciences, chemistry, or related fields, often supported by a relevant degree and laboratory experience. Familiarity with analytical instruments (such as HPLC, GC, and dissolution testers), formulation software, and Good Laboratory Practice (GLP) or Good Manufacturing Practice (GMP) guidelines is typically required. Strong attention to detail, problem-solving skills, and effective teamwork are essential soft skills in this role. These competencies ensure accurate formulation design, regulatory compliance, and the successful development of safe and effective drug products.

What are some common challenges faced by a research associate formulation development, and how can they be managed?

Research Associates in Formulation Development often encounter challenges such as optimizing formulations to achieve the desired stability, efficacy, and manufacturability. Balancing multiple project timelines and adapting to changes in experimental protocols can also be demanding. Effective communication with cross-functional teams, meticulous documentation, and staying current with new technologies are key strategies for managing these challenges. Additionally, being proactive in troubleshooting and seeking mentorship from experienced colleagues can help navigate complex formulation problems.

What is the difference between Research Associate Formulation Development vs Research Associate Quality Control?

AspectResearch Associate Formulation DevelopmentResearch Associate Quality Control
CredentialsBachelor's/Master's in Pharmacy, Chemistry, or related fieldBachelor's/Master's in Chemistry, Biology, or related field
Work EnvironmentLaboratories focused on formulation and product developmentLaboratories conducting testing and quality analysis
Industry UsagePharmaceutical and biotech companies involved in product formulationManufacturing and quality assurance departments in pharma
Common Search IntentUnderstanding formulation roles and responsibilitiesComparing quality control roles and tasks

Research Associate Formulation Development focuses on creating and optimizing drug formulations, while Research Associate Quality Control emphasizes testing and ensuring product quality. Both roles are essential in pharmaceutical development but differ in their primary functions and work environments.

What cities are hiring for Research Associate Formulation Development jobs?

Cities with the most Research Associate Formulation Development job openings:

What states have the most Research Associate Formulation Development jobs?

States with the most job openings for Research Associate Formulation Development jobs include:

What are popular job titles related to Research Associate Formulation Development jobs?

For Research Associate Formulation Development jobs, the most frequently searched job titles are:

Infographic showing various Research Associate Formulation Development job openings in the United States as of September 2026, with employment types broken down into 1% Internship, 1% As Needed, 82% Full Time, 14% Part Time, and 2% Contract. Highlights an 87% Physical, 2% Hybrid, and 11% Remote job distribution.

Associate Director/Director, Formulation & Downstream Process Development

San Diego, CA • On-site

Pivotal
See more jobs at Pivotalexternal

$80 - $100/hr

Other

Medical, Dental, Vision, Life, Retirement, PTO

Posted 22 days ago

Job description

Research Associate, Formulation Development

Location: San Diego, CA

Job Type: Full-Time, Onsite

About Us

We are an innovative, stealth-mode biotech focused on developing best-in-class delivery for in vivo gene editing.

Job Summary

We are seeking a highly motivated and skilled individual to join our team as a Research Associate in Formulation Development. The successful candidate will be responsible for designing, executing, analyzing, and making recommendations on research protocols for lipid nanoparticle (LNP) drug delivery systems aimed at gene editing. Title level and salary will be commensurate with experience.

Responsibilities
  • Develop lipid nanoparticle (LNP) formulations for gene editing applications.
  • Conduct experiments to optimize formulation parameters such as particle size, encapsulation efficiency, and stability.
  • Optimize production processes to improve yields and scalability.
  • Troubleshoot and resolve issues related to formulation processes.
  • Perform analytical characterization of LNPs using techniques such as dynamic light scattering (DLS), zeta potential measurement, and electron microscopy.
  • Support in vitro and in vivo studies to evaluate the efficacy and safety of LNP formulations.
  • Collaborate with preclinical and clinical teams to ensure successful translation of formulations.
  • Maintain accurate and detailed laboratory records.
  • Prepare technical reports and presentations to communicate findings.
  • Stay current with advancements in LNP technologies and methodologies.
Qualifications
  • Bachelor's degree or higher in Chemistry, Pharmaceutics, Biochemistry, Biomedical Engineering, Chemical Engineering, or a related field.
  • 3+ years of experience in pharmaceutical formulation, with a focus on lipid nanoparticle drug delivery systems.
  • Experience with techniques such as DLS, zeta potential measurement, and other analytical tools used in nanoparticle characterization.
  • Strong analytical and problem-solving skills.
  • Excellent communication and teamwork abilities.
  • Ability to work independently and manage multiple tasks effectively.
Preferred Qualifications
  • GMP production experience.
  • Familiarity with regulatory requirements and quality control in bioprocessing.
Benefits
  • Competitive salary, equity, and benefits package.
  • Opportunities for professional growth and development.
  • Fast paced collaborative and innovative work environment.
  • We offer an exceptional benefits package to include Medical, Dental, Vision, Life, Disability, a 401k Match of 4%, Paid Time Off and Equity.
Equal Opportunity Employer

We are an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. All employment decisions are based on business needs, job requirements, and individual qualifications, without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, veteran, or disability status.

Salary Range

$65,000 - $100,000

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