R&D Labeling & Technical Documentation Specialist
Listed on 2026-10-06
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Research/Development
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Healthcare
GForce Life Sciences seeks a detail-oriented Business Professional - Analyst, R&D Technical Writing, to develop and review labeling documentation for medical devices. You will ensure materials meet GMP and QSR standards and align with regulatory expectations to support patient safety and customer satisfaction.
This role emphasizes independent work, collaboration with R&D, Legal, Regulatory, and Quality, and effective communication across cross-functional teams to maintain accurate, compliant
As a R&D Labeling & Technical Documentation Specialist, you will play an important part at GForce Life Sciences in Salt Lake City, UT, United States.
We are currently recruiting a R&D Labeling & Technical Documentation Specialist for our team in Salt Lake City, UT, United States.
This is a strong position to take on the R&D Labeling & Technical Documentation Specialist role at GForce Life Sciences.
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