Senior Writer - Medtech Surgery

Johnson & Johnson

Raritan, New Jersey, United States of America
Base: $109,000.00 - $174,800.00; bonus/equity: not...
Fully remote
Clinical evaluation reports/plans (cer/cep)
Summary of safety and clinical performance reports (sscp)
Systematic literature reviews
Johnson & Johnson is seeking a Senior Writer for their Medtech Surgery team, responsible for creating Clinical Evaluation Reports and related documentation. The ideal candidate should have experience in the medical device industry and strong communication skills, with a focus on regulatory compliance and clinical research

Job Summary

  • Our Surgery team will give you the chance to deliver surgical technologies and solutions to surgeons and healthcare professionals around the world.
  • You will be responsible for planning, writing, and reviewing CEPs, CERs (including State of the Art protocols and reviews), Literature reports, and SSCPs.
  • The anticipated base pay range for this position is : $109,000.00 - $174,800.00

Matching Summary

Match Score: 85

Johnson & Johnson is seeking a Senior Writer for their Medtech Surgery team, responsible for creating Clinical Evaluation Reports and related documentation. The ideal candidate should have experience in the medical device industry and strong communication skills, with a focus on regulatory compliance and clinical research.

Salary

Base: $109,000.00 - $174,800.00; Bonus/Equity: Not specified; Benefits: Vacation –120 hours per calendar year, Sick time - 40 hours per calendar year, Holiday pay –13 days per calendar year, Work, Personal and Family Time - up to 40 hours per calendar year, Parental Leave – 480 hours, Bereavement Leave – 240 hours/40 hours, Caregiver Leave – 80 hours, Volunteer Leave – 32 hours, Military Spouse Time-Off – 80 hours

Skills & Requirements

Must-have

  • Clinical Evaluation Reports/Plans (CER/CEP)
  • Summary of Safety and Clinical Performance Reports (SSCP)
  • Systematic literature reviews
  • Post-Market Surveillance
  • FDA Reports
  • State of the Art (SOA) generation
  • Utilizing statistical analysis tools

Nice-to-have

  • Mentoring junior writers
  • Process efficiency improvement
  • Continuing education participation
  • Subject matter authority during audits

Key Requirements

  • Bachelor's Degree required
  • 4+ years of related experience required
  • Medical device/pharmaceutical industry experience
  • Knowledge of global clinical evaluation regulatory requirements

Work Rights

Not specified

Tailored Resume

Cover Letter