Senior Technical Writer
Apply NowCompany: RICEFW Technologies, Inc.
Location: Saint Paul, MN 55106
Description:
Job Purpose
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
Quality Systems Duties and Responsibilities:
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.
Qualifications
Additional Job Specific Requirements:
Required Skills : Adobe Creative Suite,Technical
Additional Skills : Desktop Publisher,Technical Writer
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
Quality Systems Duties and Responsibilities:
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.
Qualifications
- Bachelor's degree plus 6+ years of related experience
- Capable of swiftly grasping intricate processes
- Ability to quickly integrate and deliver high quality product output
- Experience technical writing in the medical device or other regulated industry
- Strong collaboration skills
- Strong problem-solving skills
- Ability to work in a fast-paced environment
- Demonstrated ability to handle multiple tasks and projects
- Attention to detail
- Ability to adapt and innovate in a changing environment
Additional Job Specific Requirements:
- Experience with a content management system or labeling system
- Experience with desktop publishing tools, preferably InDesign and other Adobe tools
- Ability to operate within complex processes
- Experience in technical writing used for translated documentation
Required Skills : Adobe Creative Suite,Technical
Additional Skills : Desktop Publisher,Technical Writer