R&D Principal Engineer - Electrophysiology

Johnson & Johnson•Irvine, CA

10d

About The Position

Johnson & Johnson is hiring for an R&D Principal Engineer– Electrophysiology to join our team located in Irvine, CA. 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/. 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 The R&D Principal Engineer will lead the R&D work-stream on life cycle management (LCM) projects that will primarily focus on cost improvements. This individual will work with other engineers and cross functional partners in supporting existing product improvement, own Design History Files for LCM projects, own Design Requirements and ensure the design and design's validated state complies with technical, quality, and regulatory compliance.

Requirements

Knowledge and skills to satisfactorily develop the responsibilities of the position.
8 to 10 years of experience, preferably related to the position.
University/Bachelors Degree in Engineering or Equivalent. Masters Degree or greater is preferred.
Strong knowledge of the medical device industry and manufacturing technologies
Familiarity with quality and regulatory systems including FDA’s Quality System Regulation, ISO13485, etc.
Must have an extensive experience in leading projects, developing processes, test methods, and in documentation writing.
Experience with tools and equipment for product design and manufacturing.
Demonstrated experience developing technological solutions for medical device products
Proficiency in SOLIDWORKS and Design of Experiments (DOE).
Familiarity with design control, engineering change orders (ECO), Corrective Actions and Preventive Actions (CAPA).
Ability to operate independently and adapt to changing requirements.
Ability to work in a fast-paced environment, managing multiple priorities from different projects.
Ability to travel 25% - 35% (Domestic and International)

Benefits

employees are eligible to participate in the Company’s consolidated retirement plan (pension) and savings plan (401(k)).
This position is eligible to participate in the Company’s long-term incentive program.
Vacation –120 hours per calendar year
Sick time - 40 hours per calendar year; for employees who reside in the State of Colorado –48 hours per calendar year; for employees who reside in the State of Washington –56 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 period10 days
Volunteer Leave – 32 hours per calendar year
Military Spouse Time-Off – 80 hours per calendar year