Skip to main content
Tallo logoTallo logo

Find Jobs

Find Jobs Near You – Available Work in Your Location

Skip to job details

Back to Results

Apply for this opportunity

To apply for this job, you'll continue to an external website or email application.

Katalyst Healthcares & Life Sciences

CQV Engineer

Job Description

CQV Engineer Katalyst Healthcares & Life Sciences - 4.0 Bellevue, NE Job Details Contract 19 hours ago Qualifications Laboratory equipment performance testing and validation Biochemical laboratory techniques Production validation processes
Full Job Description Responsibilities:
CQV resources supporting an NPD large-cap project modifying existing equipment and processes for future methods in an existing large-scale cell culture facility. Focus on process equipment on the floor, walking systems down, and executing qualifications and related documentation. All validation documentation and execution in ValGenesis (e-validation platform), including one documentation-focused resource.
Most Important Skills Needed:
Strong CQV experience with process equipment; able to work independently, set their own pace and goals, and still maintain team structure on second shift. Hands-on execution of IQ and OQ and traditional qualification activities, including: Walking drawings down and verifying against field configuration. TOPs for materials certifications. Verifying maintenance systems are active. Verifying process flow paths and operation per functional design. Wet testing. SIP/CIP cycle development for flow paths in coordination with manufacturing engineering.
Post-IQ/OQ activities:
Steam-in-place temperature mapping. BI (biological indicator) training and retrieval. Pulling process data and working with QC lab reports. Generating, executing, and reporting on validation documentation in ValGenesis.
Experience / comfort working with:
Large-scale cell culture (20kL bioreactor; batches 8 16kL).
Downstream equipment:
harvest clarification, viral filtration, ultrafiltration, buffer transfer, tank farms, chromatography. Steam clean-in-place activities. Strong GDP and project timeline execution; ability to support compressed schedule with 2 3 shift coverage. No CSV or lab validation required (process/CQV focus only).

Career Insights for Validation Specialist

See where this job fits in the broader career landscape. Knowing your career path helps you see what's possible from here.

Scorecard

Based on Nebraska data

Review key factors to help you decide if this role fits your goals. How is this calculated?

Were these scores useful?

What they do

A Validation Specialist tests and documents the validity and accuracy of manufacturing systems and equipment. Tests processes and manages process validations. Provides technical support and implements operating procedures. May create documentation to show that a manufacturing or production process has consistent results and meets quality standards.

$92,582 / year median in Nebraska

+7% projected growth

Explore Career