Instagram
youtube
Facebook

Technical Writer

6โ€“8 years
$105,000 โ€“ $169,050 USD
10 Sept. 10, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/ B.Pharma/ M.Pharma/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

โœ๏ธ 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
๐Ÿ”— Apply Now


๐Ÿข 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.

๐Ÿ”— Learn more: https://www.jnj.com
๐Ÿ”— About MedTech: https://www.jnj.com/medtech


๐Ÿ“„ 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.


โœ… Key Responsibilities

โœ๏ธ 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.

๐Ÿ› ๏ธ 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.

๐Ÿง  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.

๐Ÿ“Š Project Alignment

  • Align label development and document creation with project timelines.

  • Participate in labeling execution planning, resolving resource conflicts, and supporting business unit goals.


๐ŸŽ“ Qualifications

๐Ÿงพ Education:

  • Bachelor’s degree (required)

๐Ÿ’ผ Experience:

  • 6–8 years of technical or medical writing experience

  • Strong project management skills with ability to manage multiple concurrent assignments

๐Ÿงฐ 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


๐Ÿ’ฒ Compensation & Benefits

๐Ÿ’ฐ Base Salary Range:

$105,000 – $169,050 USD

๐ŸŽ 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

๐Ÿ•’ 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

๐Ÿ”— Full Benefits Info: Johnson & Johnson Careers – Benefits


๐ŸŒ 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.

๐Ÿ’ฌ For applicants requiring accommodations, visit:
๐Ÿ”— https://www.jnj.com/contact-us/careers


๐Ÿท๏ธ Tags

#LI-Hybrid #MedicalWriting #TechnicalWriter #DITA #MedicalDevices #CCMS