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Qc Analytical Associate
Posted on March 17, 2025
- Santa Monica, United States of America
- 58286.0 - 76647.0 USD (yearly)
- Contract
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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 Type: Contract
Schedule:
- 8 hour shift
- Day shift
- Monday to Friday
Experience:
- ELISA: 4 years (Required)
- Flow cytometry: 4 years (Required)
- GMP environment: 4 years (Required)
Shift availability:
- Day Shift (Preferred)
Ability to Commute:
- Santa Monica, CA 90406 (Required)
Ability to Relocate:
- Santa Monica, CA 90406: Relocate before starting work (Required)
Work Location: In person
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