Duration: 6 Months
Job Type: Contract
Work Type: Onsite
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 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.
Skills: gmp,microsoft office,troubleshooting,quality control,cytometry,instrumentation,purchase financing,elisa,sops,analytical testing,flow cytometry,manufacturing,pcr