Planet Pharma
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https://www.propharmagroup.com
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Target PR Range: 27-37/hr
*Depending on experience
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 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.
Fully Onsite Role
Quality Control Research Associate - II
Posted: 11/12/2024
2024-11-12
2025-01-04
Employment Type:
Contract
Job Category: Quality and Compliance
Job Number: 615981
Is job remote?: No
Country: United States
Job Description
Target PR Range: 27-37/hr
*Depending on experience
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 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.
Fully Onsite Role
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