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).

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