R&D Labeling & Technical Writing Analyst (USC/GC)

Matlen Silver

Salt Lake City, Northern (UT, KY)

Hybrid

USD 60,000 - 90,000

Full time

14 days+
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Benefits offered by this job

Health, vision, and dental insurance (
401(k) plan

Job summary

Matlen Silver is seeking an R&D Technical Writing Analyst to help develop and maintain labeling documentation, drawings, change orders, and specifications, ensuring GMP and QSR compliance. You will design labeling using templates and manage records in the document control system.

The role requires collaboration with R&D, Legal, Regulatory Affairs, Design Assurance, Quality, Manufacturing, and Operations to support patient safety and product quality.

Qualifications

  • Must have a detail-oriented mindset and strong change-control discipline.
  • Experience creating and managing labels in regulated environments is required.
  • Familiarity with label software tools (Prism, Label Creator, Bartender, Nice Label, Easy Label) is preferred.

Responsibilities

  • Assist in developing and maintaining labeling documentation, drawings, change orders, and specifications to GMP/QSR standards.
  • Design labeling using templates and style guides; manage digital/hardcopy records in document control systems.
  • Collaborate with R&D, Legal, Regulatory Affairs, Design Assurance, Quality, Manufacturing and Operations to support patient safety and customer satisfaction.
  • Ensure labeling changes are data-supported and aligned with applications and processes.
  • Uphold Quality Policy and support updates to SOPs and training materials.

Skills

Detail-oriented
Change control
Label creation experience

Tools

Prism
Label Creator
Bartender
Nice Label
Easy Label

Job description

Matlen Silver is seeking an R&D Technical Writing Analyst to help develop and maintain labeling documentation, drawings, change orders, and specifications, ensuring GMP and QSR compliance. You will design labeling using templates and manage records in the document control system.

The role requires collaboration with R&D, Legal, Regulatory Affairs, Design Assurance, Quality, Manufacturing, and Operations to support patient safety and product quality.

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