Sr Research Associate QC Req 8320 and 8321

This individual will support the reference st&ard, raw materials & drug substance analysis group. Primary responsibility will be reference st&ard, drug substance & raw material release. The job requires knowledge of HPLC & other general laboratory characterization experiments (IR, DSC, GC, TGA, titrations, NMR, etc.)

This individual must be able to plan & execute assigned experiments that support QC release & project goals. They must be able to work independently, as well as, in a team environment to meet critical company deadlines. This individual must be able to troubleshoot analytical instrumentation & perform calibration & maintenance as required & maintain accurate laboratory records, be detailed oriented & well organized.

This individual will also perform a variety of experiments that support research activities in other analytical groups & will need to be able to help develop & independently develop analytical methods to characterize & quantitate small molecules.

The position requires 1-2 years of relevant experience in quantitative analysis & cGMP.

The c&idate will have a Bachelors or Masters in analytical chemistry or a related field & a basic knowledge of modern analytical techniques (HPLC GC, IR, UV, KF, DSC, TGA, XRD, SEM etc.).
The c&idate will join a team of analytical chemists supporting the development of drug c&idates.