Quality Control Research Associate II - Integrated Resources, Inc
Santa Monica, CA 90404
About the Job
Job Title: Quality Control Research Associate II
Job Location: Santa Monica, CA
Job Duration: 6 Months (Possible extension)
PAYRATE- $32 - $35/hr. on w2
MOST IMPORTANT PART: Conduct Quality Control Analytical 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.
Job Description:
All previous level plus:
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.
#sczr2
Job Location: Santa Monica, CA
Job Duration: 6 Months (Possible extension)
PAYRATE- $32 - $35/hr. on w2
MOST IMPORTANT PART: Conduct Quality Control Analytical 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.
Job Description:
All 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 software.
- Writes and executes protocols and reports.
- Evaluates equipment for purchase and performs installations and qualifications of the new instruments.
- Conduct Quality Control Analytical 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.
#sczr2
Source : Integrated Resources, Inc
