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.
# Support operational systems (e.g. equipment maintenance, reagent
preparation, forms control, etc.) # May participate in method and
equipment qualifications. # Collaborate with other internal
departments efficiently and effectively (e.g. Analytical and
Pharmaceutical Sciences, QA, etc.) # Support authorship and revisions
of departmental SOPs.
Job Requirements: # Minimum education required for this position is an
Associates Degree in a scientific discipline (e.g. Analytical
Chemistry, Biochemistry, Chemistry, Biology, etc.) # Minimum
experience required for this position is 0 – 2 years of relative
laboratory experience in a GMP environment (preferred). Must
demonstrate competency with basic laboratory skills, including
documentation. # Other requirements include good communication and
organizational skills; basic computer skills (Microsoft Word and
Excel).
Thank you,
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