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Date: 19-Jul-2007
Pharmaceutical Scientist
Responsibilities
This individual will be responsible for developing Phase I/II/III
clinical formulations in-house, with subsequent supervision of outside
resources to manufacture these products for Phase I/II/III clinical
testing. You will use preformulation information to manufacture
prototype formulations, identifying both a dosage form composition and
a process for automated manufacturing, and then coordinate the
manufacture of the dosage forms at contract manufacturing sites,
providing bulk dosage forms for clinical and stability studies. You
will also coordinate project tasks and timelines with Analytical R&D,
Process Chemistry, QC, and other departments and prepare do***entation
for regulatory filings. Experience required 5 - 7 Years
Experience and other requirements
Requires a BS, MS or PhD in Pharmaceutical Sciences, Chemical
Engineering, or a related discipline and 4-6 years of industrial
pharmaceutical experience, or PhD Formulator with 2-4 years of
industrial pharmaceutical experience, including demonstrated
responsibility for development and manufacture of oral solid liquid
and oral liquid dosage forms. Experience with development and
manufacturing of IV solutions and modified release solids is desired,
not not required. Scientist has extensive knowledge of cGMPs; superior
technical writing skills, particularly in the preparation of batch
record and IND do***ents; computer proficiency in Word and Excel, and
excellent communication and organizational skills. Approximately 25%
travel time will be required. Minimum education requirements
Bachelors
Thank you,
BioTech FYI Center
http://biotech.fyicenter.com/
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