Senior Scientist - JJMT Electrophysiology
About The Position
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: Medical Affairs Group Job Sub Function: Medical Affairs Job Category: Scientific/Technology All Job Posting Locations: Irvine, California, United States of America Job Description: Our J&J MedTech Electrophysiology Medical Affairs team is currently recruiting for a Senior Scientist. This position is located in Irvine, California. 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/. 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 Cardiovascular? Ready to join a team that’s 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 https://www.jnj.com/medtech Job Responsibilities: This Medical Affairs Senior Scientist will be responsible for supporting one or several product development projects within the JJMT EP’s product portfolio while fostering strong, productive relationships with colleagues across the organization. Under general direction and in accordance with all applicable federal, state and local laws/regulations and Corporate Johnson & Johnson, procedures and guidelines, this position is: Responsible for executing the clinical strategy to support product characterization and design features Will develop and execute product and/or procedural protocols for evidence generation Collaborate with evidence generation colleagues for evidence generation for new and existing products in order to support regulatory approval/clearance Provide scientific and test method expertise during study design development Provide pre-clinical insight to the development teams for the risk assessment
Requirements
- BS with at least 6 years, MS with at least 4 years, PhD with at least 2 years of relevant experience in Engineering, Life Sciences, Physical Sciences, Nursing, or Biological Science is required.
- An understanding of cardiac anatomy and medical devices are required.
- A minimum of 3 years working on pre-clinical models is required, with chronic models is preferred.
- Advanced technical writing skills is required with an emphasis on organizing data and presenting findings, with a demonstrated success in medical data generation, interpretation, and publications are highly preferred
- A proven working knowledge of catheter laboratory equipment and operating room procedures
- Experience in working with a global cross-functional teams is required.
- Must be able to work in a high stress environment with minimal supervision.
- Proven project management skills, with a demonstrable track record of success managing multiple projects
- Must be able to collaborate well with multiple partners and work effectively in a matrix environment
Responsibilities
- Responsible for executing the clinical strategy to support product characterization and design features
- Will develop and execute product and/or procedural protocols for evidence generation
- Collaborate with evidence generation colleagues for evidence generation for new and existing products in order to support regulatory approval/clearance
- Provide scientific and test method expertise during study design development
- Provide pre-clinical insight to the development teams for the risk assessment
Benefits
- employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).
- Vacation –120 hours per calendar year
- Sick time - 40 hours per calendar year
- Holiday pay, including Floating Holidays –13 days per calendar year
- Work, Personal and Family Time - up to 40 hours per calendar year
- Parental Leave – 480 hours within one year of the birth/adoption/foster care of a child
- Bereavement Leave – 240 hours for an immediate family member: 40 hours for an extended family member per calendar year
- Caregiver Leave – 80 hours in a 52-week rolling period
- Volunteer Leave – 32 hours per calendar year
- Military Spouse Time-Off – 80 hours per calendar year
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Number of Employees
5,001-10,000 employees
