Senior Quality Engineer NPI LCM

At Johnson & Johnson,we believe health is everything.

Our strength in healthcare innovation empowers us to build aworld where complex diseases are prevented, treated, and cured,where 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 jnj.com .

As guided by Our Credo, Johnson & Johnson is responsible to our employees who work with us throughout the world.

We provide an inclusive work environment where each person is considered as an individual.

At Johnson & Johnson, we respect the diversity and dignity of our employees and recognize their merit.

Job Function:
Quality

Job Sub Function:
R&D/Scientific Quality

Job Category:
Professional

All Job Posting Locations:
Irving, Texas, United States of America

Job Description:

J&J MedTech is recruiting for a Senior Quality Engineer New Product Innovation & Lifecycle Management (NPI/LCM) to join our Aesthetics & Reconstruction (A&R) organization located in Irving, Texas.

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

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

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

The Senior Quality Engineer NPI LCM is responsible for supporting product quality and reliability ensuring the implementation of ground-breaking technology for medical devices is safe, effective, and follows applicable regulations, standards, and industry practices.

Working closely with multi-functional teams, this individual will support product quality throughout the product lifecycle for both new product introductions and lifecycle management.

The individual reviews and assesses development activities (e.g., user needs, development / quality plans, requirements, risk management, verification and validation) to ensure that they align with applicable procedures standards and regulatory requirements.

Additional responsibilities may include but are not limited to supporting other areas of the Quality Management System such as CAPA, Complaints, post market surveillance and both Internal & External Audits.

DUTIES & RESPONSIBILITIES

Responsibilities:


* Support launch and stabilize new product launches through concept, design, development, and steady-state processes.


* Drives the development of product requirements, verification strategies, and validation strategies.


* Ensures new product development compliance to GMP (Good Manufacturing Practices), ISO (International Organization for Standardization) and any other applicable standards


* Activities would drive prevention, detection of defects at earliest phase of product design, continuous improvement & customer satisfaction.


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