βοΈ Technical Writer
Job Title: Senior Analyst, Medical Writing (P6)
Location: Cincinnati, Ohio, United States
Work Type: Hybrid
Date Posted: September 8, 2025
Application Deadline: September 22, 2025 (may be extended)
Requisition Number: R-031587
π Apply Now
π’ About Johnson & Johnson
At Johnson & Johnson, we believe that health is everything. We are a global leader in healthcare innovation, focused on creating smarter, less invasive, more personalized treatments across MedTech and Innovative Medicine.
π Learn more: https://www.jnj.com
π About MedTech: https://www.jnj.com/medtech
π Position Summary
We are hiring a Technical Writer (Sr. Analyst, Medical Writing) to join our Medical Affairs Group. This role will be based in Cincinnati, OH and work within the Medical Writing sub-function, producing clear, compliant, and user-centric documentation for medical devices and regulated products.
β Key Responsibilities
βοΈ Document Creation & Management
Write, review, and revise technical content:
User manuals
Standard Operating Procedures (SOPs)
Service manuals, packaging inserts, and training materials
Translate complex technical data into accessible, user-friendly language.
Maintain and update documents in response to product changes, regulatory updates, or design improvements.
Ensure compliance with global regulatory standards (e.g., FDA, ISO 13485, MDR).
Generate and release document part numbers using the Product Lifecycle Management (PLM) system.
π οΈ Systems, Tools, and Platforms
Work within a DITA-based CCMS (Component Content Management System).
Act as system administrator and manage integrations (e.g., Acrolinx).
Author content using XML, following topic-based (DITA) methodology.
Support translation efforts across global documentation.
π§ Content Leadership & Mentorship
Contribute to establishing a consistent product taxonomy and editorial voice.
Mentor junior writers in content planning, use-case delivery, and best practices.
Collaborate cross-functionally to restructure IFU templates for better scalability and efficiency.
π Project Alignment
Align label development and document creation with project timelines.
Participate in labeling execution planning, resolving resource conflicts, and supporting business unit goals.
π Qualifications
π§Ύ Education:
Bachelor’s degree (required)
πΌ Experience:
6–8 years of technical or medical writing experience
Strong project management skills with ability to manage multiple concurrent assignments
π§° Preferred Skills:
Knowledge of the medical device industry or other regulated sectors
Familiarity with quality systems and change control procedures
Demonstrated experience with:
PLM systems
DITA/XML authoring
CCMS platforms
Content translation workflows
π² Compensation & Benefits
π° Base Salary Range:
$105,000 – $169,050 USD
π Benefits Include:
(Subject to eligibility and company plans)
Medical, Dental, Vision insurance
Life insurance, Business Accident, Disability insurance
401(k) and Pension plans
Long-Term Incentive Program
π Time-Off Benefits:
Vacation: 120 hours/year
Sick Leave: 40–56 hours/year (based on location)
Holidays: 13 paid days/year
Parental Leave: 480 hours within 1 year of childbirth/adoption
Volunteer Time: 4 days/year
Caregiver Leave: 10 days
Condolence Leave: Up to 30 days
Military Spouse Leave: 80 hours/year
Work, Personal & Family Time: Up to 40 hours/year
π Full Benefits Info: Johnson & Johnson Careers – Benefits
π Diversity, Inclusion & Accommodations
Johnson & Johnson is an Equal Opportunity Employer. We value diversity and do not discriminate based on race, color, religion, gender, age, disability, sexual orientation, or veteran status.
π¬ For applicants requiring accommodations, visit:
π https://www.jnj.com/contact-us/careers
π·οΈ Tags
#LI-Hybrid #MedicalWriting #TechnicalWriter #DITA #MedicalDevices #CCMS
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