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  Structure Data Format (SDF) Related Website Resources         


Author: http://biotech.fyicenter.com
Date: Jan 11, 2007 08:50

Structure Data Format (SDF) Related Website Resources

http://biotech.fyicenter.com/resource/sdf_format.html

Structure Data Format (SDF) is a chemical file formats to represent
multiple chemical structure records and associated data fields. SDF was
developed and published by Molecular Design Limited (MDL) and became
the the most widely used standard for importing and exporting
information on chemicals.

Please visit:
go to http://biotech.fyicenter.com/resource/sdf_format.html

Thank you,
BioTech FYI Center
http://biotech.fyicenter.com/
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  US-MO-St Charles: Associate Scientist in biotech         


Author: http://biotech.fyicenter.com
Date: Jan 11, 2007 08:49

To apply for this position, please visit this Website.
http://biotech.fyicenter.com/jobs/99897490_Associate_Scientist_in_biotech.html
To see other BioTech job opportunities, please visit
http://biotech.fyicenter.com/
Date: 11-Jan-2007

/corporate/careers.nsf/home

Associate Scientist in biotech

RESPONSIBILITIES - Develops new immunoassays (RIA, EIA, Multiplex),
formulas, processes, methods for resolution of technical problems. -
Develops, characterizes, and purifies antibodies. - Development...
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  US-MA-Worcester: QC Scientist         


Author: http://biotech.fyicenter.com
Date: Jan 11, 2007 08:47

To apply for this position, please visit this Website.
http://biotech.fyicenter.com/jobs/99897481_QC_Scientist.html
To see other BioTech job opportunities, please visit
http://biotech.fyicenter.com/
Date: 11-Jan-2007

QC Scientist

Job Description Assist with method transfer and validation activities
as well as support routine testing. Write and revise SOP's and
validation protocols. Individual must be able to accurately follow oral
and written procedures in operating basic laboratory equipment and
performing testing procedures. This position requires the individual to
be flexible and be able to handle multiple tasks on a routine basis.
Skills/Experience Requirements Minimum of 5 years of related work
experience in a GMP environment.

Strong technical writing (i.e., method transfer and validation
protocols, SOP's), LIMS experience, strong communication skills. Prior
experience in HPLC and ELISA's preferred. Experience with protein
analytics required.
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