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QC Lab Technician

Job in Mission, Johnson County, Kansas, 66201, USA
Listing for: Exothera
Full Time position
Listed on 2025-11-29
Job specializations:
  • Healthcare
    Data Scientist
Salary/Wage Range or Industry Benchmark: 55000 - 75000 USD Yearly USD 55000.00 75000.00 YEAR
Job Description & How to Apply Below
Position: QC Lab Technician - Exothera

Every person will have the opportunity to contribute to our mission and be impactful. Apply and be part of this great adventure!

MISSION

We are currently looking for Quality Control (QC) Laboratory Technicians with proven expertise in Droplet Digital PCR (ddPCR) and ELISA to join our fast-growing team. In this role, you will contribute directly to the quality and reliability of our viral vector products by performing critical release and stability testing in a GMP-regulated environment.

You will be part of a dynamic QC team working at the intersection of innovation and rigorous quality standards. Your work will support upstream and downstream production teams by delivering reliable analytical results and insights that drive key decisions in our bioproduction pipeline.

RESPONSIBILITIES
Analytical Execution

Prepare and perform quantitative molecular biology assays, primarily ddPCR
.

Perform additional plate-based and molecular QC tests as required.

Prepare reagents, calibrate equipment, and validate methods according to SOPs and GMP regulations.

Ensure accurate and complete documentation of test results following Good Documentation Practices (GDP).

Reporting & Data Analysis

Analyze ddPCR and ELISA data and communicate results to QC Scientists and other stakeholders.

Assist in compiling test reports, deviation investigations, and trend analyses.

Support troubleshooting and continuous improvement initiatives.

Maintenance & Inventory

Perform routine maintenance, calibration, and troubleshooting of ddPCR and ELISA instrumentation.

Ensure appropriate stock levels of reagents, consumables, and standards.

Contribute to lab organization, cleanliness, and compliance.

Documentation & Training

Participate in writing and reviewing SOPs, protocols, and method validation documents.

Provide training to new team members on ddPCR and ELISA platforms.

Share technical knowledge and participate in cross-functional discussions.

REQUIREMENTS & QUALIFICATIONS

Bachelor’s or Master’s degree in Molecular Biology, Biochemistry, Biotechnology, or a related field.

Minimum 2 years of hands-on experience with ddPCR (Bio-Rad or similar platforms) in a GMP or regulated environment.

Strong technical troubleshooting and data interpretation skills.

Practical mindset with a strong sense of laboratory discipline and organization.

Comfortable working both independently and in a team in a fast-paced, multi-tasking environment.

Strong written and verbal communication skills (English required).

Curiosity-driven and eager to contribute to continuous improvement.

Join us and be part of a collaborative, high-impact team advancing the future of cell and gene therapies!

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