Qc Research Associate

3 weeks ago


Santa Monica, United States TekwissenGroup Full time

**Job Description ** **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 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 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 Types**: Full-time, Contract

Pay: $30.00 - $35.00 per hour

Application Question(s):

- How many years of experience do you have with ELISA and flow Cytometry? (minimum 2 years)
- How many years of experience do you have with QC Raw material testing? (minimum 2 years)
- Do you have a bachelor's degree?

Work Location: In person



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