Description:
All of previous level plus:Conduct non-routine analysis of raw materials intermediates and finished product instrumentation and test in the training of QC staff as knowledge of current Good Manufacturing Practices (cGMPs) and Good Laboratory Working knowledge and proficiency with Microsoft Office and executes protocols and equipment for purchase and performs installations and qualifications of the new instruments.
Conduct Quality Control Analtyical testing (e.g. ELISA Flow Cytometry PCR) of patient samples stability samples controls and reagent qualification in a GMP environment. Perform reviews of assays and maintain laboratory in a state of compliance.
Troubleshoot instrumentation and test in the training of QC staff as knowledge of current Good Manufacturing Practices (cGMPs) and Good Laboratory Working knowledge and proficiency with Microsoft Office and executes protocols and SOPs.
MOST IMPORTANT PART: Conduct Quality Control Analtyical testing (e.g. ELISA Flow Cytometry PCR) of patient samples stability samples controls and reagent qualification in a GMP environment. Perform reviews of assays and maintain laboratory in a state of compliance.