Description:
12 months contract with the possibility to extend
Onsite
Location Santa Monica CA 90404
All of previous level plus:Conduct nonroutine analysis of raw materials intermediates and finished product samples.Troubleshoot instrumentation and test methods.Assists in the training of QC staff as needed.Applies knowledge of current Good Manufacturing Practices (cGMPs) and Good Laboratory Working knowledge and proficiency with Microsoft Office software.Writes and executes protocols and reports.Evaluates 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 methods.Assists in the training of QC staff as needed.Applies knowledge of current Good Manufacturing Practices (cGMPs) and Good Laboratory Working knowledge and proficiency with Microsoft Office software.Writes 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.
Fully Onsite Role