Consultant Scientist

3 weeks ago

Louisville, United States CYNET SYSTEMS Full time
Job Description:

Pay Range $60hr - $90hr

Responsibilities:
  • The CMC Pharmaceutics team has an exciting opportunity for an innovative individual to join our organization and develop the growing oncology portfolio of therapeutic small molecules.
  • The individual will be responsible for aspects of API physicochemical characterization, preclinical and clinical drug product formulation development, and stability testing.
  • Work collaboratively with pharmaceutics, process chemistry, and analytical chemistry teams to deliver data that supports oncology program development.
  • Plan and conduct experiments on pre-formulation, characterization of API, and the design of formulations such as suspensions, solutions, tablets, capsules, and spray-dried dispersions.
  • Assist in the development of appropriate analytical test methods and stability studies for drug product formulations.
  • Maintain laboratory notebook, laboratory equipment, and chemical inventory.
  • Provide written and verbal updates on assigned projects and activities as required.
  • Author and review technical documents and formulation development reports.
Qualifications:
  • Ph.D. in pharmaceutics, chemistry, material science, chemical engineering, or related discipline with 0-2 years experience, a Master s degree with 1-3 years of experience, or a Bachelor s degree with 1-5 years of pharmaceutical industry experience.
  • Excellent scientific knowledge in pre-formulation, material science, and formulation.
  • Experience with chemistry techniques, solubility determination, compatibility studies, formulation screening, dissolution, polymorph screening, and physicochemical characterization of API as well as formulations.
  • Demonstrated ability to work well with other accomplished professionals within and across functions/teams.
  • Strong written and oral communication skills.
  • Experience with pharmaceutical data interpretation.
  • Demonstrable ability to work proactively, independently, and tenaciously.
  • Experience in instrumental techniques such as XRPD, DSC, TGA, DVS, HPLC, SEM, and Dissolution is highly desired.
  • Experience in the formulation, process development, and manufacturing of drug products.
  • Ability to multi-task and shift priorities rapidly to meet tight deadlines.
  • Detail-oriented and well-organized, good and thoughtful listener.
  • Enthusiastic, self-motivated, and keen to improve processes, overcome inefficiencies, and able to adapt to changing environments with ease.
  • Proficient in Microsoft Office suite and applications.

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