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Research And Development Associate

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Job Description

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.

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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.

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Qualifications of the R&D Associate:

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

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  • Design and develop innovative formulations, such as tablets and gummies.
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  • Optimize formulations for improved stability, bioavailability, and patient adherence.
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  • Ensure all formulations adhere to regulatory guidelines and industry standards.
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  • Understand and apply 21 CFR FDA drug compliance requirements.
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  • Perform HPLC stability testing, dissolution tests, and other essential evaluations to confirm formulation safety and effectiveness.
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  • Develop prototypes and samples for further testing and validation.
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  • Analyze experimental data and draw insights to drive formulation improvements.
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  • Maintain accurate, detailed records of all experiments and outcomes.
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  • Ensure formulations align with internal quality benchmarks.
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  • Implement quality control processes throughout the formulation development lifecycle.
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  • Collaborate effectively with teams such as quality control, regulatory, and production.
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  • Communicate progress, challenges, and results clearly to stakeholders.
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  • Stay informed on the latest trends in pharmaceutical formulation and evolving regulatory standards.
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Occupational code: 19-2031.00 (Chemists)

Vacancy posted 9 days ago
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