Senior Technical Writer - MedTech Surgery

At Johnson & Johnson, we believe health is everything.

Our strength in healthcare innovation empowers us to build a world where complex diseases are prevented, treated, and cured, where treatments are smarter and less invasive, and solutions are personal. Through our expertise in Innovative Medicine and MedTech, we are uniquely positioned to innovate across the full spectrum of healthcare solutions today to deliver the breakthroughs of tomorrow, and profoundly impact health for humanity. Learn more at https://www.jnj.com

Job Function:
R&D Operations

Job Sub Function:
Clinical/Medical Operations

Job Category:
Professional

All Job Posting Locations:
Raritan, New Jersey, United States of America, Remote (US)

Job Description:

About Surgery

Fueled by innovation at the intersection of biology and technology, we’re developing the next generation of smarter, less invasive, more personalized treatments.

Are you passionate about improving and expanding the possibilities of surgery? Ready to join a team that’s reimagining how we heal? Our Surgery team will give you the chance to deliver surgical technologies and solutions to surgeons and healthcare professionals around the world.

Your contributions will help effectively treat some of the world’s most prevalent conditions such as obesity, cardiovascular disease and cancer.

Patients are waiting.

Your unique talents will help patients on their journey to wellness.

Learn more at https://www.jnj.com/medtech

We are searching for the best talent for a Senior Technical Writer to support our Surgery business.  Remote work options may be considered on a case-by-case basis and if approved by the Company.  There is a strong preference for candidates in Eastern or Central time zones.

Purpose: The Sr.

Technical Writer provides oversight and execution of Clinical Evaluation Reports/Plans (CER) and Summary of Safety and Clinical Performance Reports (SSCP) for Ethicon Endo-Surgery within J&J Global R&D Medical Device sector.

You will be responsible for:


* Planning and writing CEPs, CERs (including State of the Art protocols and reviews) and SSCPs


* Mentoring junior writers.


* Conducting technical reviews to ensure document accuracy and compliance to local procedures, J&J guidelines and regulatory requirements.


* Partnering with cross-functional team members to address needs of each contributor.


* Leading daily activities to ensure timelines are met.


* Participating in workshops and other initiatives to help define and continuously improve process efficiency.


* Participating in continuing education activities to improve understanding of associated regulatory requirements and industry trends/practices.


* Supporting and, at times, acting as a subject matter authority during audits and inspections pertaining to processes and reports.


* Responsible for communicating business related issues or opportunities to next management level.


* For those w...