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Search for Jobs by Brandon Haas

Research Scientist (Science & Biotech)
South San Francisco, CA 94080
Recruited by: Brandon Haas | Manager of Operations | TalentMine See all my Jobs

  • Hiring Company: TalentMine
  • Industry: Science & Biotech
  • Compensation: to be determined
  • Expires: Feb 10, 17
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Job Description

Duties:
• Has applicable experience in formulation technologies for solid/liquid oral dosage forms not limited to high shear granulation, roller compaction, fluid bed granulation, spray drying, tableting, and capsule filling.
• Evaluate physic-chemical characteristics of small molecules such as pH, pKa, solubility, pH-solubility profile, particle size, solid and solution state stability studies, dissolution characteristics and polymorphism.
• Has experience on optimization and scale-up of process/formulations (solid/liquid) for clinical studies.
• Has demonstrated experience in successfully working with Clinical Manufacturing Organizations (CMOs) to oversee manufacturing to support clinical trials. Responsibilities include the preparation review and the approval of a broad spectrum of technical documents, including Manufacturing Batch Reports (MBRs), specifications, protocols, reports, etc.


Education/Experience Required:
• BS/BA degree in bioengineering, biophysics, chemical engineering, pharmaceutics, or pharmaceutical sciences and seven years of related experience; or,
• MS/MA degree in bioengineering, biophysics, chemical engineering, pharmaceutics, or pharmaceutical sciences, and five years of related experience; or
• PhD in bioengineering , biophysics, chemical engineering, pharmaceutics, or pharmaceutical sciences, and three years of related experience, or;
• Equivalent combination of education and experience
• May require certification in assigned area
• Experience in Biotech/Pharmaceutical industry preferred including with pediatric formulation development.
• Must have proven skills in the areas formulated development and process optimization


KNOWLEDGE/SKILLS/ABILITIES:
• Strong knowledge of and experience of the various phases of drug development for oral dosage forms is required.
• Able to manage project assignments and function in a driven and fast moving team environment.
• Familiarity and working knowledge of current Good Manufacturing Practices (cGMP)/International Conference on Harmonization (ICH) regulations, with experience working in a GMP facility is required.
• Experience with statistical tools to design and evaluate experiments for formulations and process development preferred.
• Proficient with broad use of computer applications such as MS Office.
• Applies strong analytical and excellent verbal and written communication skills.