Summary :
- Execute experiments for the formulation and QC of oral and parenteral vehicles for in vivo evaluation of novel lead materials.
- Prepare and deliver accurate formulation of test articles to achieve experimental goals. Conduct solid form characterization including thermodynamic solubility, particle size, polyform characterization, melting point, salt equivalent determination, and water content analysis to advance lead compounds toward candidate nomination.
- Work closely with experts in medicinal chemistry, DMPK, pharmacology, and technical operations to generate key data that drive understanding of ADMET properties and test article pharmacology.
- Partner with Technical Operations and CMC teams to develop prototype formulations and processes for non-GLP pre-clinical studies in advanced research programs.
- Operate state-of-the art analytical instruments, such as Agilent HPLC 1260, waters LCMS, PLM, and Rigaku Miniflex XRPD.
- Track formulation activities under tight timelines, ensuring cross-functional collaboration and accountability.
Must haves :
- Master's with 2+ years, or Bachelor’s with 5+ years of relevant experience in an academic, biotech, or pharmaceutical industry
- Degree in Pharmaceutics, Pharmaceutical Sciences, Chemistry, Analytical Chemistry, Biochemistry, Chemical Engineering, or related discipline
- Proven experience in developing and optimizing oral and / or parenteral, formulations of small molecules for the characterization of ADMET properties or in vivo pharmacology
- Hands on experience with HPLC analysis, stability testing, and physicochemical property determination. Familiarity with solid form characterization techniques, including PLM, TGA, DSC, XRPD, and Dissolution preferred.
- Strong experimental design skills for various dose formulations, along with expertise in developing methods for drug materials with low solubility.
- Exceptional attention to details and experience in protocol writing experience for accurately recording experimental parameters and procedures.
- Excellent communication, organization, time management, and documentation skills. Ability to work both independently and collaboratively.
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Execute experiments for the formulation and QC of oral and parenteral vehicles for in vivo evaluation of novel lead materials. Prepare and deliver accurate formulation of test articles to achieve experimental goals. Partner with Technical Operations and CMC teams to develop prototype formulations an...
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The Senior Research Scientist II will be responsible for lead optimization, API form selection/characterization, pre-formulation, formulation development, manufacture of clinical supplies, development of efficient and scalable manufacturing processes, process scale up based on Quality by Design (QbD...
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The Senior Research Scientist II will be responsible for lead optimization, API form selection/characterization, pre-formulation, formulation development, manufacture of clinical supplies, development of efficient and scalable manufacturing processes, process scale up based on Quality by Design (QbD...
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The Senior Research Scientist I will be responsible for lead optimization, API form selection/characterization, pre-formulation, formulation development, manufacture of clinical supplies, development of efficient and scalable manufacturing processes, process scale up based on Quality by Design (QbD)...
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The Senior Research Scientist I will be responsible for lead optimization, API form selection/characterization, pre-formulation, formulation development, manufacture of clinical supplies, development of efficient and scalable manufacturing processes, process scale up based on Quality by Design (QbD)...