Owns creation, execution, and maintenance of technical documentation for Smith+Nephew's New Product Development and other projects. This role collaborates with various functions to understand, develop, and maintain all aspects of technical documentation across projects.
• Develop (research/write/illustrate) content, including understanding and communicating detailed technical concepts
• Work closely with R&D Engineering, Regulatory, Quality, and Marketing to create any new project-related technical documentation and to make ongoing updates that are a result of user feedback, review of risk management file, and to support regulatory and quality compliance.
Responsibilities:
• Produces technical documentation including user manuals, package inserts, and other technical guides.
• Analyzes and updates existing and new documents to maintain continuity with regulations and project needs.
• Designs labels based on input from cross-functional team.
• Confers with project managers, engineers, and regulatory experts to establish technical specification, determine text and illustrations to be developed for publication, and ensure accuracy of product documentation.
• Determines technical documentation priorities based on timelines and resource capacity.
• Anticipates potential project problems and creates solutions or contingency plans.
• Manages workload across multiple projects.
Required Qualifications:
o High-tech, medical device labeling and documentation development experience preferred
Other Qualifications, Skills & Certifications:
All your information will be kept confidential according to EEO guidelines.