Remote Medical Writer Jobs at Johnson and Johnson | Apply Now
The demand for skilled Remote Medical Writer Jobs professionals is rapidly rising across the global healthcare industry, and Johnson & Johnson is offering an exceptional opportunity for experts seeking impactful work in medical writing, scientific operations, and regulatory documentation. This fully remote role is ideal for candidates exploring Johnson & Johnson career options, high-quality remote jobs, or competitive Jobs in USA within the MedTech and Innovative Medicine landscape.
About Johnson & Johnson
At Johnson & Johnson, we believe health is everything. Our strength in healthcare innovation drives us to create a world where diseases are prevented, treated, and cured through smarter, less invasive, and personalized solutions. Through Innovative Medicine and MedTech, we are uniquely positioned to deliver breakthroughs that profoundly impact global health.
Job Details:
- Job Title: Medical and Technical Writer, Scientific Operations
- Function: Medical Affairs Group
- Sub-Function: Medical Writing
- Category: Experienced Analyst (P5)
- Location: Irvine, CA / Irving, TX / United States (Fully Remote Option Available)
- Requisition Number: R-045164
- Work Pattern: Fully Remote
- Application Deadline: Nov 28, 2025 (may be extended)
About MedTech
Driven by innovation at the intersection of biology and technology, MedTech develops next-generation, less invasive, and highly personalized treatments that support every stage of the patient journey.
Position Overview
Johnson & Johnson is seeking a Medical and Technical Writer, Scientific Operations (SciOps) for the MedTech Neurovascular business unit. Remote work may be considered. An internal candidate has been identified, but all applicants will be fully considered. You will lead the development of medical and technical documents—including CERs, SOAs, literature reviews, SSCPs, and PSURs—to support regulatory submissions, compliance, and market access.
Key Responsibilities
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Develop a wide range of SciOps documents:
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Clinical Evaluation Plan (CEP)
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Clinical Evaluation Report (CER)
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Literature Review Protocol (LRP)
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Literature Review Report (LRR)
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Summary of Safety and Clinical Performance (SSCP)
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Periodic Safety Update Report (PSUR)
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Related medical/technical assessments
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Respond to Health Authority and Notified Body inquiries.
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Track and analyze inquiries to improve processes and accelerate market access.
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Ensure alignment with relevant Quality Systems and Regulatory documentation (Risk Management, PMS, etc.).
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Collaborate across functions: Medical Affairs, Clinical Research, Quality, R&D, Regulatory Affairs.
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Participate in workshops and improvement initiatives.
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Support audits and inspections related to SciOps processes and reports.
Required Qualifications
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Bachelor’s degree in Life Sciences, or related discipline.
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Minimum 3 years of industry experience (medical device, diagnostics, or pharma).
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At least 1 year of experience in:
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Medical/technical writing
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Regulatory writing
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Post-market surveillance
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Clinical research
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Product risk management
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Preferred Qualifications
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Advanced degree: MS, PhD, RN, MBA.
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Knowledge of neurovascular physiology and device outcomes.
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Familiarity with EU MDR requirements (clinical evaluation, state of the art, data sufficiency).
Compensation & Benefits of Remote Medical Writer Jobs
Base Pay Range: $109,000 – $148,000
Eligible for:
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Annual performance-based bonus
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Medical, dental, vision insurance
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Life, disability, accident & legal insurance
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Pension plan and 401(k)
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Time-off benefits including:
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120 hours vacation
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40 hours sick time (56 hours for WA residents)
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13 paid holidays including floating holidays
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40 hours Work/Personal/Family Time
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480 hours parental leave
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Caregiver, volunteer, bereavement, and military spouse leave
More details available at: careers.jnj.com/employee-benefits
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Required Skills for Remote Medical Writer Jobs
Clinical Research, Medical Writing, Post-Marketing Surveillance, Product Risk Management, Regulatory Writing
Preferred Skills
Business Writing, Clinical Research Operations, Coaching, Collaboration, Copy Editing, Data Analysis, Document Management, Industry Knowledge, Problem Solving, Quality Standards, Research Ethics, Technical Writing, Medical Communications
