Analysis Skills, Cardiac Monitoring, Cardiology, Communication Skills, Content Development, Content Management, Continuous Improvement, Cross-Functional, Customer Relations, Customer Support/Service, Documentation Review, International Marketing, Maintain Compliance, Marketing Objectives, Patient Safety, Process Improvement, Product Documentation, Product Safety, Regulations, Regulatory Compliance, Sales, Team Player, Technical Writing
Cardiac Rhythm Management Technical Communications
You will work collaboratively with development teams to create customer-facing manuals and labels necessary to support our client's worldwide regulatory, marketing, and sales objectives. By joining our Cardiac Rhythm Management Technical Communications team, your work will be a part of the life-saving products used around the world. This person will be assisting with an ICM Tablet project.
Key Responsibilities
- Plan, analyze, and create content using technical writing theories, methods, and tools
- Assist with administrative authoring tasks, including routing documents for approvals, and reviewing documents for accuracy and conformance to standards and regulations
- Interpret and apply Boston Scientific processes to ensure compliance with regulatory and standard-based requirements
- Ensure document content quality by managing and organizing information for accuracy, consistency, and readability
- Establish and manage content across different documents and product types in a manner that promotes consistency and efficiency
- Identify, analyze, recommend, and implement innovative solutions to drive continuous improvement in technical writing processes and practices
- Collaborate with a cross-functional team to update Instructions for Use for a cardiac diagnostic device
- Effectively communicate updates to cross-functional teams and gather their feedback for integration into the labeling process
In all actions, demonstrates a primary commitment to patient safety and product quality by maintaining compliance to the Quality Policy and all other documented quality processes and procedures.