Kelly
This range is provided by Kelly. Your actual pay will be based on your skills and experience — talk with your recruiter to learn more.
Base pay range $28.00/hr - $40.00/hr
Direct message the job poster from Kelly
Kelly® Science & Clinical is seeking a Quality Control Analyst for a 6-month contract opportunity with one of our clients, a leading cell therapy biotechnology at their Louisville, CO facility. 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.
Overview Step into a pivotal Quality Control (QC) Analyst/Senior Analyst role with our cutting-edge QC Analytical team, supporting pioneering therapies at the forefront of cellular medicine.
As a key member of our client’s early-phase QC group, you’ll work cross-functionally and immerse yourself in a fast-paced, start-up environment where every contribution accelerates life-changing therapies toward the clinic.
Workplace:
Onsite in Louisville, CO
Contract:
6 months
Compensation:
Analyst: $28–$33/hr
Sr Analyst: $33–$40/hr
What You’ll Do:
Advance Tomorrow’s Therapies:
Perform QC analytical testing for product release, stability, and in-process controls under expert guidance, ensuring the highest standards for cell and gene therapy products.
Drive Innovation:
Collaborate with Analytical Development teams on method qualification, transfer, and troubleshooting—bringing your QC expertise to solve complex assay challenges.
Champion Quality and Compliance:
Manage sample receipt, aliquoting, and custody with precision, supporting seamless manufacturing and QC operations.
Lead Operational Excellence:
Participate in and promote Continuous Improvement (CI), applying CI principles to refine QC workflows in a regulated lab setting.
Own Your Work:
Take independent responsibility for daily lab activities such as inventory, reagent qualification, and cell passaging—critical building blocks of high‑quality therapies.
Expand Your Impact:
Support QC Microbiology, stability timepoint management, and other cross‑functional initiatives as needed, gaining exposure to the full spectrum of quality operations.
Who Thrives Here:
Analyst Level: Bachelor’s degree in Biochemistry, Molecular & Cellular Biology, Immunology, or related life science, plus 1+ year experience in cGMP‑quality control—or an equivalent blend of education and relevant experience.
Senior Analyst Level: Same scientific background plus 2+ years hands‑on QC experience in cGMP‑regulated labs.
Experience & Attributes:
Proven record managing molecular QC assays: dPCR, ELISA, Flow Cytometry, and cell‑based testing
Deep familiarity with cGMP documentation, pharmaceutical regulations, and industry best practices
Passion for teamwork, dedication to purpose, and drive to champion an exceptional workplace
Unmatched collaborative spirit and willingness to share knowledge
Preferred Qualifications:
Startup experience in laboratory buildout, quality systems, or analytical method development
Hands‑on with molecular and cell‑based assays—digital PCR, Flow Cytometry, ELISA, and more
Background in cell and gene therapy manufacturing/testing environments
What happens next: Once you apply, you’ll proceed to the 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.
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Base pay range $28.00/hr - $40.00/hr
Direct message the job poster from Kelly
Kelly® Science & Clinical is seeking a Quality Control Analyst for a 6-month contract opportunity with one of our clients, a leading cell therapy biotechnology at their Louisville, CO facility. 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.
Overview Step into a pivotal Quality Control (QC) Analyst/Senior Analyst role with our cutting-edge QC Analytical team, supporting pioneering therapies at the forefront of cellular medicine.
As a key member of our client’s early-phase QC group, you’ll work cross-functionally and immerse yourself in a fast-paced, start-up environment where every contribution accelerates life-changing therapies toward the clinic.
Workplace:
Onsite in Louisville, CO
Contract:
6 months
Compensation:
Analyst: $28–$33/hr
Sr Analyst: $33–$40/hr
What You’ll Do:
Advance Tomorrow’s Therapies:
Perform QC analytical testing for product release, stability, and in-process controls under expert guidance, ensuring the highest standards for cell and gene therapy products.
Drive Innovation:
Collaborate with Analytical Development teams on method qualification, transfer, and troubleshooting—bringing your QC expertise to solve complex assay challenges.
Champion Quality and Compliance:
Manage sample receipt, aliquoting, and custody with precision, supporting seamless manufacturing and QC operations.
Lead Operational Excellence:
Participate in and promote Continuous Improvement (CI), applying CI principles to refine QC workflows in a regulated lab setting.
Own Your Work:
Take independent responsibility for daily lab activities such as inventory, reagent qualification, and cell passaging—critical building blocks of high‑quality therapies.
Expand Your Impact:
Support QC Microbiology, stability timepoint management, and other cross‑functional initiatives as needed, gaining exposure to the full spectrum of quality operations.
Who Thrives Here:
Analyst Level: Bachelor’s degree in Biochemistry, Molecular & Cellular Biology, Immunology, or related life science, plus 1+ year experience in cGMP‑quality control—or an equivalent blend of education and relevant experience.
Senior Analyst Level: Same scientific background plus 2+ years hands‑on QC experience in cGMP‑regulated labs.
Experience & Attributes:
Proven record managing molecular QC assays: dPCR, ELISA, Flow Cytometry, and cell‑based testing
Deep familiarity with cGMP documentation, pharmaceutical regulations, and industry best practices
Passion for teamwork, dedication to purpose, and drive to champion an exceptional workplace
Unmatched collaborative spirit and willingness to share knowledge
Preferred Qualifications:
Startup experience in laboratory buildout, quality systems, or analytical method development
Hands‑on with molecular and cell‑based assays—digital PCR, Flow Cytometry, ELISA, and more
Background in cell and gene therapy manufacturing/testing environments
What happens next: Once you apply, you’ll proceed to the 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.
#J-18808-Ljbffr