Quality System Specialist

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

Quality

Job Sub Function

Quality Systems

Job Category

Professional

All Job Posting Locations:

Yokneam, Haifa District, Israel

Job Description

About Cardiovascular

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

We are searching for a talented quality and compliance specialist to be in Yokneam

This role is responsible for serving as the internal processes improvement agent and maintaining quality system comprehensive compliance.

In This Role You Will Be

• Responsible for management and effectiveness of the CAPA process.
• Responsible for periodic monitoring of documents approaching the review period and notifications to document owners
• Organize and lead the Data Review Boards and Quality Systems Management Review.
• Responsible for maintaining updated list of applicable J&J internal standards
• Assist in the development of quality metrics in order to achieve company's quality goals.
• Performs other duties assigned as needed
  
  

• A minimun of Degree in engineering or life science.
• At least 3 years quality background, including previous roles.
• Experience as quality Specialist and/or quality assurance Specialist responsible for CAPA execution in medical devices and/or pharmaceutics company
• Ability to build strong working relationship with internal partners
• Experience managing international multi-disciplinary projects.
• Qualification in Quality Assurance as Quality Auditor, ISO and QSR standards/regulations for the medical devices or pharmaceutics industries (preferred)