Medical & Technical Writer, Sci Ops JJMT Electrophysiology

At Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions are 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 more at

Job Function : R&D Operations

Job Sub Function :

Clinical / Medical Operations

Job Category : Professional

All Job Posting Locations :

Irvine California United States of America Raritan New Jersey United States of America

Job Description :

Johnson & Johnson MedTech Electrophysiology is recruiting an Medical & Technical Writer to join our Scientific Operations team. This role can be located in Irvine California or Raritan NJ with a hybrid working schedule of 2-3 days per week on-site.

Johnson & Johnsonwe believe health is everything. Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented treated and curedwhere treatments are smarter and less invasive andsolutions 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 by innovation at the intersection of biology and technology were developing the next generation of smarter less invasive more personalized treatments.

Are you passionate about improving and expanding the possibilities of Cardiovascular Ready to join a team thats reimagining how we heal Our Cardiovascular team develops leading solutions for heart recovery electrophysiology and stroke. You will join a proud heritage of continually elevating standards of care for stroke heart failure and atrial fibrillation (AFib) patients.

Your unique talents will help patients on their journey to wellness. Learn more at the Medical & Technical Writer within Scientific Operations (SciOps) you will lead the authoring of Clinical Evaluations (CERs) State of the Art Assessments (SOA) Literature Reviews Summaries of Safety and Clinical Performance (SSCP) and Periodic Safety Updates (PSUR) for the MedTech Electrophysiology business unit. You will also provide input and support to related functions ensuring the delivery of key regulatory and medical documents to gain and retain market access.

Job Responsibilities :

Write Scientific Operations medical and technical documentation including Clinical Evaluation Plan (CEP) Clinical Evaluation Report (CER) Literature Review Protocol (LRP) Literature Review Report (LRR) Summary of Safety and Clinical Performance (SSCP) Periodic Safety Updates Report (PSUR) documents and other medical and technical assessments based on available data inputs.

Respond to inquiries from Health Authorities and Notified Body as it pertains to data and information presented in the documents written. Track and trend inquiries and responses to improve processes and increase speed to market. Translate insights into viable processes and solutions that create value.

Ensure the Scientific Operations deliverables are linked to appropriate Quality Systems and Regulatory documents (e.g. Risk Management PMS etc.) to make certain information is consistent and accessible where needed.

Communicate to drive alignment in strategy across different functions including Medical Affairs Clinical Research Quality R&D and Regulatory Affairs.

Participate in workshops and projects / initiatives to help define processes improvements.

Support audits and inspections pertaining to Scientific Operations processes and reports.

Qualifications

Required :

Minimum of a Bachelors degree (University Degree) in Life Sciences Engineering or related subject area.

Minimum of 3 years of experience medical device diagnostics or pharmaceutical industry with one of those years directly involved with medical devices.

One year of experience in technical or medical writing regulatory writing post market surveillance clinical research or product risk management.

Preferred :

Knowledge of physiology and common outcomes of electrophysiology

An advanced degree MS PhD RN or MBA.

Familiarity with the EU MDR regulations as it pertains to clinical evaluations data sufficiency requirements and state of the art assessments.

Johnson & Johnson is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity age national origin disability protected veteran status or other characteristics protected by federal state or local law. We actively seek qualified candidates who are protected veterans and individuals with disabilities as defined under VEVRAA and Section 503 of the Rehabilitation Act.

Johnson & Johnson is committed to providing an interview process that is inclusive of our applicants needs. If you are an individual with a disability and would like to request an accommodation external applicants please contact us via . Internal employees contact AskGS to be directed to your accommodation resource.

Required Skills : Preferred Skills :

Clinical Evaluation Reports Clinical Operations Clinical Research and Regulations Clinical Trial Designs Literature Reviews Medical Device Industry

The anticipated base pay range for this position is :

$92000 - $148000

Additional Description for Pay Transparency :

The Company maintains highly competitive performance-based compensation programs. Under current guidelines this position is eligible for an annual performance bonus in accordance with the terms of the applicable plan. The annual performance bonus is a cash bonus intended to provide an incentive to achieve annual targeted results by rewarding for individual and the corporations performance over a calendar / performance year. Bonuses are awarded at the Companys discretion on an individual basis. Employees and / or eligible dependents may be eligible to participate in the following Company sponsored employee benefit programs : medical dental vision life insurance short- and long-term disability business accident insurance and group legal insurance. Employees may be eligible to participate in the Companys consolidated retirement plan (pension) and savings plan (401(k)). This position is eligible to participate in the Companys long-term incentive program. Employees are eligible for the following time off benefits : Vacation up to 120 hours per calendar year Sick time - up to 40 hours per calendar year; for employees who reside in the State of Washington up to 56 hours per calendar year Holiday pay including Floating Holidays up to 13 days per calendar year Work Personal and Family Time - up to 40 hours per calendar year Additional information can be found through the link below.

Key Skills

Clinical Research,Adobe Acrobat,FDA Regulations,Technical Writing,Biotechnology,Clinical Development,Clinical Trials,Microsoft Powerpoint,Research Experience,Document Management Systems,Word Processing,Writing Skills

Employment Type : Full-Time

Experience : years

Vacancy : 1

Monthly Salary Salary : 92000 - 148000