US-MA-Norwood: Quality Control Analyst Chemistry
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Date: 12-Aug-2008
Quality Control Analyst I, Chemistry
Description: The Quality Control Analyst I will provide support to GMP
manufacturing of multiple clinical programs through performance of
simple to moderately complex release, in-process, and stability
testing for drug substance and drug product. Expected support and
contributions to general laboratory operations, documentation
practices, and quality system improvements. Ability to contribute to
laboratory initiatives and learn technical / troubleshooting skills.
This position requires flexibility with changing priorities.
# Key responsibilities and tasks include, but are not limited to:
Performance of QC analytical testing (e.g. quality assays,
electrophoresis, etc.) on drug substance and drug product for release
and stability across multiple programs; may also include raw material
testing, sampling, and labeling, as needed.
