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Research Associate

Clinical Research Associate III
Company: Sanofi
1 Year
Framingham,MA
Max PR:$27 - $30.65/hr

Responsibilties:
The incumbent will join a dynamic multi-disciplinary multi-modality drug product development team, with responsibilities that span from formulation development to fill finish of clinical, commercial and life-cycle stage assets within the Biologics/GMU Drug Product Development and Manufacturing.

The successful candidate would be required to:
o Develop experimental plans and execute studies to assess physicochemical stability of non-viral, viral vectors- and cell-based therapeutics
o Assist in process development studies for manufacturing unit operations for injectable dosage forms (e.g. freeze-thaw, mixing, filtration, filling, lyophilization etc.).
Assist in developing new technologies in the areas of polymer-based drug delivery technologies
o Work closely and independently with counterparts from other functional areas to deliver on CMC milestones
o Generate, document and compile data for team and senior management discussions and draft development reports
o Mentor junior staff as required

Education & Qualifications
  • BS in Chemical Engineering, Pharmaceutical Science, Analytical Chemistry, Biochemistry, Biology (or related discipline)

Preferred Qualifications
  • Solid understanding and practical experience in drug product formulation and process development of non-viral gene therapeutics: formulation development of lipid nanoparticles, liposomes and polymer conjugates for nucleic acid delivery, container closure selection, stability studies, in-use studies and process development of liquid, frozen, and lyophilized drug product.
  • Theoretical knowledge and hands-on experience in analytical techniques: Fluorescence based nucleic acid quantitation assays (e.g. Ribogreen assay), HPLC/UPLC, capillary electrophoresis, gel electrophoresis, DLS, zeta-potential, DSC, DSF, UV, CD, Cryo-TEM.
  • Experience in formulation and process development of viral vector-and cell-based therapeutics is a plus.
  • Experience in cell culture, flow-cytometry, qPCR, ITA, plate-based potency assay is a plus.
  • Basic understanding of statistical data analysis. Good written and verbal communication skills.