R&D Labeling & Technical Documentation Specialist

GForce Life Sciences

Salt Lake City (UT)

On-site

USD 60,000 - 90,000

Full time

2 days ago

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Benefits offered by this job

Job summary

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

Qualifications

Bachelor’s degree or equivalent practical experience.
Understanding of GMP and QSR labeling standards.
Proficiency with GLS/Prisym, Adobe CS, and MS Office.
Experience with Zebra printers and barcode tools.
Ability to work in cross-functional teams with accuracy.

Responsibilities

Develop, review, and maintain labeling documentation per regulatory standards.
Design labeling layouts using GLS/ Prisym and Adobe CS.
Collaborate with R&D, Regulatory, Legal, and other teams.
Verify printed labels and troubleshoot printer issues.
Maintain records in PLM and other data systems.
Update SOPs and technical docs with graphics.

Skills

Attention to detail

Cross-functional collaboration

Technical writing

Regulatory knowledge

Communication skills

Education

Bachelor's degree

Tools

GLS/Prisym

Adobe Creative Suite

Microsoft Office

Zebra printers

Barcode verification tools

Job description

This role emphasizes independent work, collaboration with R&D, Legal, Regulatory, and Quality, and effective communication across cross-functional teams to maintain accurate, compliant

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