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QC Analyst

Phoenix Metro Area, Arizona

Post Date: 05/24/2017 Job ID: JN -052017-19134
Responsibilities:
Translation of site environmental monitoring activities for aseptic manufacturing facility into templates for capture of viable and non-viable results.
Assist in integration of laboratory instrumentation with LabWare to support both environmental monitoring and routine microbiology laboratory activities.

Skills/Knowledge:
BS Chemistry/Microbiology or relevant discipline with equivalent experience.
Minimum 5 years recent cGMP/GLP pharmaceutical laboratory experience.
Minimum 5 years direct experience with implementation of LIMS specific to environmental monitoring of aseptic manufacturing facilities. LabWare implementation preferable or MODA implementation acceptable.
Subject Matter Lead for implementation of at least 1 LIMS electronic environmental monitoring solution.
Good laboratory documentation skills and thorough understanding of cGMP documentation requirements.
Good communication skills.
Strong collaboration skills to enable team to achieve results.
Sound scientific judgment based on reasonable assumptions and available information.

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