Technical Writer

Technical Writer

Remote

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.

Looking for a Sr level Technical Writer with substantial experience to join our team, capable of quickly getting up to speed to kickstart work on an ICM (Insertable Cardiac Monitor) Tablet project with a tight deadline. This role will be creating customer facing manuals and labels to support our client's worldwide regulatory, marketing, and sales objectives.

Med device experience strongly preferred.

Key experience we're looking for is content management system or labeling system, plus experience with desktop publishing tools, preferably InDesign and other Adobe tools

location: Remote position - US based.

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

Job Type: Full-time

Salary: $45.00 - $50.00 per hour

Expected hours: 50 per week

Schedule:

• 8 hour shift

Experience:

• Adobe InDesign: 10 years (Required)
• Technical writing: 10 years (Preferred)
• Content management systems: 10 years (Required)
• medical devices: 10 years (Required)

Work Location: Remote