IntePros is currently seeking a qualified R&D Technical Writing Analyst to support the development, maintenance, review, and implementation of labeling and technical documentation within a medical device environment. This role will work closely with cross-functional teams to ensure documentation is accurate, compliant, consistent, and appropriate for its intended audience.
Responsibilities:
• Develop, review, and maintain labels, drawings, specifications, change orders, SOPs, Work Instructions, forms, and technical documentation.
• Create and revise labels using approved templates, labeling systems, Adobe products, and Microsoft Office.
• Manage records within document control and PLM systems.
• Review labeling changes for accuracy, compliance, and supporting documentation.
• Support label verification, barcode grading, printing, troubleshooting, and production implementation.
• Coordinate documentation reviews and approvals across R&D, Regulatory Affairs, Quality, Manufacturing, Operations, Legal, and Marketing.
• Track project tasks, resolve documentation issues, and support quality system compliance.
Qualifications:
• Bachelor’s degree or equivalent education and practical experience.
• Experience with technical writing, labeling, document control, PLM systems, or medical device documentation preferred.
• Proficiency with Microsoft Office and Adobe products.
• Strong attention to detail, organization, communication, and project coordination skills.
• Familiarity with GLS, Prisym, Zebra printers, barcode graders, GMP, QSR, or quality systems is a plus.