Compunnel Inc.
Quality Control Analyst (Lab Support)
Compunnel Inc., Boulder, Colorado, United States, 80301
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Position Overview
This range is provided by Compunnel Inc. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range
$20.00/hr - $22.00/hr Responsibilities
Conduct routine preparations for stability, raw materials, in-process, microbiology/ cleaning validation program and other requested testing according to Standard Operating Procedures (SOP) and Analytical Methods in accordance with current Good Manufacturing Practices (cGMPs) and regulatory requirements Complete projects with supervision and have a clear understanding of Good Laboratory Practices (GLPs), CGMPs, and other regulatory requirements Ability to exercise judgment and appropriately raises issues to QC management Key focus will be preparing solutions (mobile phase, diluent, etc) and standard/sample preparations Required to follow good documentation practices Works cross-functionally to complete projects and testing Qualifications
Bachelor’s required in life science Generally, requires minimal to no prior relevant work experience Demonstrated knowledge of analytical equipment and instrumentation and working in a GMP environment is helpful Proven skills in coordinating and leading day to day tasks and working in collaboration to accomplish deadlines and objectives Seniority level
Mid-Senior level Employment type
Contract Job function
Engineering and Quality Assurance Industries
Biotechnology Research, Medical Equipment Manufacturing, and Research Services
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This range is provided by Compunnel Inc. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more. Base pay range
$20.00/hr - $22.00/hr Responsibilities
Conduct routine preparations for stability, raw materials, in-process, microbiology/ cleaning validation program and other requested testing according to Standard Operating Procedures (SOP) and Analytical Methods in accordance with current Good Manufacturing Practices (cGMPs) and regulatory requirements Complete projects with supervision and have a clear understanding of Good Laboratory Practices (GLPs), CGMPs, and other regulatory requirements Ability to exercise judgment and appropriately raises issues to QC management Key focus will be preparing solutions (mobile phase, diluent, etc) and standard/sample preparations Required to follow good documentation practices Works cross-functionally to complete projects and testing Qualifications
Bachelor’s required in life science Generally, requires minimal to no prior relevant work experience Demonstrated knowledge of analytical equipment and instrumentation and working in a GMP environment is helpful Proven skills in coordinating and leading day to day tasks and working in collaboration to accomplish deadlines and objectives Seniority level
Mid-Senior level Employment type
Contract Job function
Engineering and Quality Assurance Industries
Biotechnology Research, Medical Equipment Manufacturing, and Research Services
#J-18808-Ljbffr