Toxikon Corporation, originally founded in 1977, is a Contract Research and testing company with laboratories in Bedford, MA. Our mission continues to focus on providing quality pre-clinical services, competitively priced, with on-time delivery for the Pharmaceutical, Medical Device and Biotech industries.
In this quality assurance role, the appropriate candidate will be responsible for the implementation, functioning, and monitoring of quality assurance activities. This includes monitoring biological and chemical studies, and creating reports in conformance with GLP practices. Candidates will review GMP, GLP and non-GLP reports for accuracy with reference to protocols, Quality Assurance Standards, Standard Operational Procedures, laboratory precision and accuracy limits, as well as reviewing all protocols for compliance and accuracy. Other quality assurance responsibilities include maintaining equipment performance, calibration records and preventative maintenance logs. Included duties are performing system and phase audits according to GLP and ISO guidelines, as well as all other activities required from quality assurance.
A bachelor’s degree in a life science is required, preferably in Biology.
Experience in a regulated testing environment with fundamental knowledge of study design and data review practices.
GLP and GMP knowledge preferred.
Must have strong documentation and coordination practices, be detail oriented and enjoy high work volume via computer.
This position is located in Bedford, MA.
For additional information about Toxikon go to www.toxikon.com.
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