Kelly Science, Engineering, Technology & Telecom
Quality Control Analyst
Kelly Science, Engineering, Technology & Telecom, Louisville, Colorado, United States, 80028
Kelly Science, Engineering, Technology & Telecom provided pay range
This range is provided by Kelly Science, Engineering, Technology & Telecom. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range $56,100.00/yr - $84,000.00/yr
Direct message the job poster from Kelly Science, Engineering, Technology & Telecom
Kell y® Science & Clinical is seeking a
Quality Control (QC) Analyst / Senior Analyst
for a 6 month
contract
position at a cutting-edge client in
Louisville, CO . If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.
Pay:
Analyst: $56,100 - $69,300
Senior Analyst: $68,000 - $84,000
Schedule:
Day Shift Full-time, on-site
Overview
This client is an industry-leading company that’s transforming the treatment of cancer with a novel integrated immunotherapy platform. Their vision is to develop off-the-shelf therapies capable of treating any tumor, any time. The team operates from brand-new facility in Louisville, CO. and is driven by groundbreaking science, technology, and a commitment to Diversity, Equity, and Inclusion.
In this role, you will join the Quality Control Analytical team to support early-phase QC operations. You’ll collaborate across functions, perform analytical testing, and contribute to method development and operational excellence in a dynamic biotech start-up environment.
Responsibilities:
Demonstrate the Client’s values as part of a high-performing, inclusive, and collaborative organization.
Perform QC analytical laboratory testing for product release, stability, and in-process testing under supervision.
Execute sample management tasks including receipt, aliquoting, and chain of custody.
Collaborate with Analytical Development for method qualification, transfer, and troubleshooting.
Participate in Operational Excellence/Continuous Improvement initiatives.
Independently manage daily lab tasks such as inventory, reagent qualification, and cell passaging.
Support QC operations including microbiology tasks and stability timepoint pulls.
Qualifications:
Bachelor’s degree in Biochemistry, Molecular and Cellular Biology, Immunology, Biology, or related life science.
Minimum 1 year in a cGMP-regulated QC environment (or equivalent education/experience).
Bachelor’s degree in Biochemistry, Molecular and Cellular Biology, Immunology, Biology, or related life science.
Minimum 2+ years in a cGMP-regulated QC environment (or equivalent education/experience).
Required Skills:
Experience in cGMP QC laboratory.
Molecular biology background including dPCR, ELISA, Flow Cytometry, and cell-based assays.
Ability to follow SOPs, methods, and protocols with basic regulatory knowledge.
Strong teamwork and commitment to purpose and culture.
Preferred Qualifications:
Experience with lab startup, quality systems, and analytical methods.
Familiarity with molecular assays and cell-based test methods.
Experience in cell and gene therapy manufacturing/testing.
QC Microbiology and aseptic technique experience.
Physical Requirements:
Ability to gown aseptically and work in a Clean Room.
Wear PPE including gloves, protective clothing, and safety glasses.
Work while gowned for extended periods.
Lift up to 20 lbs regularly.
What happens next:
Once you apply, you’ll proceed to next steps if your skills and experience look like a good fit. But don’t worry – even if this position doesn’t work out, you’re still in our network. That means our team of expert Science & Clinical recruiters will have access to your profile, making your opportunities limitless.
Seniority level Associate
Employment type Full-time
Job function Quality Assurance and Science
#J-18808-Ljbffr
Base pay range $56,100.00/yr - $84,000.00/yr
Direct message the job poster from Kelly Science, Engineering, Technology & Telecom
Kell y® Science & Clinical is seeking a
Quality Control (QC) Analyst / Senior Analyst
for a 6 month
contract
position at a cutting-edge client in
Louisville, CO . If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.
Pay:
Analyst: $56,100 - $69,300
Senior Analyst: $68,000 - $84,000
Schedule:
Day Shift Full-time, on-site
Overview
This client is an industry-leading company that’s transforming the treatment of cancer with a novel integrated immunotherapy platform. Their vision is to develop off-the-shelf therapies capable of treating any tumor, any time. The team operates from brand-new facility in Louisville, CO. and is driven by groundbreaking science, technology, and a commitment to Diversity, Equity, and Inclusion.
In this role, you will join the Quality Control Analytical team to support early-phase QC operations. You’ll collaborate across functions, perform analytical testing, and contribute to method development and operational excellence in a dynamic biotech start-up environment.
Responsibilities:
Demonstrate the Client’s values as part of a high-performing, inclusive, and collaborative organization.
Perform QC analytical laboratory testing for product release, stability, and in-process testing under supervision.
Execute sample management tasks including receipt, aliquoting, and chain of custody.
Collaborate with Analytical Development for method qualification, transfer, and troubleshooting.
Participate in Operational Excellence/Continuous Improvement initiatives.
Independently manage daily lab tasks such as inventory, reagent qualification, and cell passaging.
Support QC operations including microbiology tasks and stability timepoint pulls.
Qualifications:
Bachelor’s degree in Biochemistry, Molecular and Cellular Biology, Immunology, Biology, or related life science.
Minimum 1 year in a cGMP-regulated QC environment (or equivalent education/experience).
Bachelor’s degree in Biochemistry, Molecular and Cellular Biology, Immunology, Biology, or related life science.
Minimum 2+ years in a cGMP-regulated QC environment (or equivalent education/experience).
Required Skills:
Experience in cGMP QC laboratory.
Molecular biology background including dPCR, ELISA, Flow Cytometry, and cell-based assays.
Ability to follow SOPs, methods, and protocols with basic regulatory knowledge.
Strong teamwork and commitment to purpose and culture.
Preferred Qualifications:
Experience with lab startup, quality systems, and analytical methods.
Familiarity with molecular assays and cell-based test methods.
Experience in cell and gene therapy manufacturing/testing.
QC Microbiology and aseptic technique experience.
Physical Requirements:
Ability to gown aseptically and work in a Clean Room.
Wear PPE including gloves, protective clothing, and safety glasses.
Work while gowned for extended periods.
Lift up to 20 lbs regularly.
What happens next:
Once you apply, you’ll proceed to next steps if your skills and experience look like a good fit. But don’t worry – even if this position doesn’t work out, you’re still in our network. That means our team of expert Science & Clinical recruiters will have access to your profile, making your opportunities limitless.
Seniority level Associate
Employment type Full-time
Job function Quality Assurance and Science
#J-18808-Ljbffr