All of previous level plus : Conduct non-routine 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 and executes protocols and reports.
Evaluates equipment for purchase and performs installations and qualifications of the new instruments.
Conduct Quality Control Analtyical testing (, 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 and executes protocols and SOPs.
MOST IMPORTANT PART : Conduct Quality Control Analtyical testing (, 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
EEO :
Quality Control Research Associate - II*
Conduct Quality Control Analtyical testing (e. Conduct Quality Control Analtyical testing (e. ELISA, Flow Cytometry, PCR) of patient samples, stability samples, controls, and reagent qualification in a GMP environment. ELISA, Flow Cytometry, PCR) of patient samples, stability samples, controls, and ...
Quality Control Research Associate
Title : Quality Control Research Associate II. Conduct Quality Control Analytical testing (e. MOST IMPORTANT PART: Conduct Quality Control Analytical testing (e. ELISA, Flow Cytometry, PCR) of patient samples, stability samples, controls, and reagent qualification in a GMP environment. ...
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