• Posted on: Sep 11, 2026
  • Location: Chicago, IL
  • Job ID: 3b1d1c4d
  • Type: Full Time
  • Posted on: Sep 11, 2026
  • Location: Chicago, IL
  • Job ID: 3b1d1c4d
  • Type: Full Time

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Our client’s cutting-edge pharmaceutical research team is on the hunt for a dynamic R&D Associate to join their ranks. They are looking for a creative problem-solver who thrives on pushing the boundaries of product development. The ideal candidate will bring a wealth of experience in formulations, conducting stability and efficacy assessments, and navigating the complex landscape of regulatory compliance.

If you have a background that blends formulation expertise with analytical chemistry or quality control know-how, we want to hear from you. Get ready to play a crucial role in shaping the future of our client’s R&D team and impacting lives.

Qualifications of the R&D Associate:

  • A Bachelor’s degree in Chemistry, Biochemistry, or a closely related discipline (MS or PhD preferred).
  • 3 to 5 years of hands-on experience in developing formulations or HPLC testing.
  • In-depth understanding of formulation techniques or analytical testing and industry practices.
  • Proficient in analytical instruments.
  • Excellent analytical and problem-solving capabilities.
  • Strong skills in organization and managing multiple projects.
  • Familiarity with regulatory standards and compliance guidelines.

Responsibilities of the R&D Associate:

  • Design and develop innovative formulations, such as tablets and gummies.
  • Optimize formulations for improved stability, bioavailability, and patient adherence.
  • Ensure all formulations adhere to regulatory guidelines and industry standards.
  • Understand and apply 21 CFR FDA drug compliance requirements.
  • Perform HPLC stability testing, dissolution tests, and other essential evaluations to confirm formulation safety and effectiveness.
  • Develop prototypes and samples for further testing and validation.
  • Analyze experimental data and draw insights to drive formulation improvements.
  • Maintain accurate, detailed records of all experiments and outcomes.
  • Ensure formulations align with internal quality benchmarks.
  • Implement quality control processes throughout the formulation development lifecycle.
  • Collaborate effectively with teams such as quality control, regulatory, and production.
  • Communicate progress, challenges, and results clearly to stakeholders.
  • Stay informed on the latest trends in pharmaceutical formulation and evolving regulatory standards.

Occupational code: 19-2031.00 (Chemists)

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