Senior Technical Writer - Instructional Labeling

System One; Denver (CO); Remote; USD 79,000 - 99,000; Full time

Job summary

A leading global medical device company seeks a Senior Content Developer to enhance their instructional labeling. This remote role requires advanced knowledge in medical products, project management skills, and proficiency in XML, offering competitive pay and comprehensive benefits.

Benefits

Excellent healthcare benefits

Paid time off

Wellness programs

Retirement plans

Qualifications

• Minimum of 7 years of experience in writing labelling for medical devices.
• Experience with process improvement initiatives.
• Ability to produce multiple required documents for projects.

Responsibilities

• Develops comprehensive instructional labeling for medical devices.
• Coordinates with subject matter experts to meet business objectives.
• Forecasts project deadlines and budgets.

Skills

Writing labelling for medical devices

Proficiency in XML

Skills in Adobe Illustrator

Project management

Content Management System (CMS)

Education

Bachelor's degree

Tools

Oxygen XML Editor

Adobe Photoshop

Adobe InDesign

Job description

Title: Senior Content Developer - Product Labeling Instructions

Location: Remote

Schedule: M-F 8:00 AM - 5:00 PM

Pay: $79,200 - $99,000 - Target Bonus on Base: 7%, inclusive (bonus, excellent healthcare benefits, PTO)

Type: Direct/Permanent

Start date: Immediate

Overview:

Our client, a global medical device company, is currently seeking qualified candidates for the position of Content Developer who will assist in creating comprehensive instructional labeling for cutting-edge medical devices for clinical and commercial products.

Responsibilities:

• Maintains advanced knowledge of the company's products and the therapies in which they are used.
• Partners with subject matter experts to develop content to achieve specific and immediate business objectives. Metrics will be used to determine the effectiveness of content.
• Understands the design control process and can complete the required documentation for a project.
• Develops content with content management systems and other tools, creates output mechanisms, and analyzes system workflow.
• Forecasts and meets project deadlines and budgets. Reports on project status and alerts managers and internal customers of potential difficulties.
• Assists in maintaining art, photo, electronic, and printed document files to meet departmental and regulatory requirements.
• Facilitates discussions and represents the Technical Communication team.
• Clarifies and maintains departmental policies and procedures.
• Seeks ongoing knowledge of industry, regulatory, linguistic, and publication standards and applies this knowledge to all projects.

Requirements:

• A bachelor’s degree or equivalent education and experience sufficient to perform the job’s essential functions.
• Minimum of 7 years of experience in writing labelling for medical devices, including writing/editing, graphic design, or project management in a heavily regulated environment.
• Supporting design controls, producing five different documents: requirements document, protocol, plan, report/summary, and final summary report.
• Proficiency in XML using Oxygen XML Editor.
• Experience working in a Content Management System (CMS) for publishing.
• Experience with process improvement initiatives and developing procedures.
• Skills in Adobe Illustrator, Photoshop, InDesign, Astoria, and knowledge of desktop publishing systems, XML, XSLT, and CSS.

The company offers comprehensive benefits, including medical, dental, vision plans, wellness programs, life insurance, disability coverage, voluntary benefits, retirement plans, and paid time off, supporting the personal and family welfare of its employees.