Careers at C.G. Laboratories

Building the Future of Medical Device Safety, Sterilization Science & Regulatory Quality

Where Service & Scientific Guidance Never Stop

At C.G. Laboratories, Inc., our team is the foundation of our 40+ year legacy in medical device testing, microbiological analysis, and sterilization validation. Founded in 1983, we have expanded into an ISO 13485:2016 and MDSAP certified dual-site facility spanning 19,000 square feet in Granbury, Texas.

We take pride in maintaining a collaborative human-to-human culture where scientists, laboratory technicians, quality assurance specialists, and operational managers work together to protect global public health.

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90+ Years Combined Expertise

Work alongside industry-leading microbiologists and sterilization experts with decades of hands-on technical experience.

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ISO 13485 & MDSAP Rigor

Gain valuable exposure to world-class Quality Management Systems and global medical device regulatory frameworks.

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Diverse Life Science Services

Engage across microbiology, contract packaging, hydrogel manufacturing, reusable device processing, and environmental monitoring.

Key Professional Disciplines at C.G. Labs

We continuously foster top-tier talent across technical, microbiological, and operational fields.

Microbiology Laboratory Testing

Perform bioburden testing, sterility evaluations, bacteriostasis/fungistasis validation, chromogenic endotoxin testing, and microbial identification for medical device products.

Sterilization & Validation Engineering

Develop, execute, and consult on protocol design for Ethylene Oxide, Steam, and E-Beam sterilization methods adhering to ISO 11135 and ISO 11137 standards.

Quality Assurance & Compliance

Maintain our ISO 13485:2016, MDSAP, and FDA compliance infrastructures, ensuring continuous audit readiness and regulatory precision across operations.

Device Decontamination & Reprocessing

Execute rapid turnaround decontamination procedures for complaint medical devices, reusable instrument washing, and automated cleaning validation.

Packaging Operations & Manufacturing

Manage sterile medical device contract packaging, sealing validation, package integrity testing, and specialized hydrogel formulation production lines.

Environmental & Facility Monitoring

Support air microbial sampling, surface monitoring programs, particle counting, and cleanroom disinfectant validation to uphold ISO cleanliness standards.

Authorized Career & Staffing Partners

For immediate employment opportunities, temporary placement, and laboratory staffing inquiries, please contact our official hiring partners directly:

KP Staffing

(817) 573-5200

Luxor Staffing

(817) 546-4950