Technical Writer – Medtronic
Company: Medtronic
Job Title: Technical Writer
Job ID: R62392
Location: Nanakramguda, Hyderabad, India
Work Arrangement: Flexible Work Arrangement
Experience: 4–7 Years
Employment Type: Full-Time
Role Overview
The Technical Writer is responsible for creating, maintaining, and managing Instructions for Use (IFUs), product labels, and technical documentation for medical devices. This role ensures that product documentation is accurate, regulatory compliant, user-friendly, and suitable for a global audience.
The position sits at the intersection of:
Medical Device Documentation
Regulatory Compliance
Product Development
Technical Communication
Translation Management
Quality Systems
The primary goal is to ensure healthcare professionals and end users receive clear instructions that support the safe and effective use of Medtronic products.
Key Responsibilities
IFU & Label Development
Create and maintain product Instructions for Use (IFUs).
Develop product labels and associated documentation.
Gather technical information from:
Product Development Teams
Engineering Teams
Marketing Teams
Regulatory Affairs Teams
Ensure documentation reflects current product design and functionality.
Documentation Management
Manage document version control.
Maintain documentation archives.
Ensure traceability of revisions.
Control documentation throughout the product lifecycle.
Regulatory Compliance
Ensure documentation complies with:
Medical device regulations
Quality management systems
Internal documentation standards
Support regulatory submissions with compliant labeling and IFUs.
Translation & Localization
Identify translation requirements for global markets.
Coordinate translation projects.
Work with external translation vendors.
Verify translated content for consistency and accuracy.
Product Lifecycle Support
Manage documentation within Product Lifecycle Management (PLM) systems.
Track documentation workflows.
Support change management activities.
Content Review & Quality Control
Proofread technical documents.
Review documentation prepared by other writers.
Ensure consistency of terminology and formatting.
Maintain documentation quality standards.
Process Improvement
Evaluate existing documentation processes.
Identify efficiency opportunities.
Implement workflow improvements.
Support continuous improvement initiatives.
Required Qualifications
Education
One of the following:
Bachelor's Degree in:
Life Sciences
Medical Sciences
Mechanical Engineering
Electrical Engineering
OR
Master's Degree in Pharmacy / Pharmaceutical Sciences
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