Operation Quality Manager

Description:

Johnson & Johnson is currently seeking a Quality Manager to join our team located in Yokneam, Israel.

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/. 

Our local company expertise in driving best-in-class solutions in cardiac ablation, stroke care and intracardiac imaging. We are looking for a Quality Manager who is responsible for planning, managing and coordinating quality assurance activities designed to ensure effective new product development, lifecycle management, product quality and supplier management.

Duties and Responsibilities:

• Leads the development and implementation of quality practices for the effective and efficient development, transfer, and maintenance of products/processes throughout the product lifecycle.
• Leads efforts with quality improvement opportunities as appropriate to legacy products, continuous improvement, and customer satisfaction.
• Ensure Compliance of product life cycle-related processes and relevant Quality procedures
• Lead the quality LCM activities such as calibration, PM, QC & Final release, non-conforming management etc.
• Attends Quality Review Board and Material Review Board meetings to provide product quality expertise and lead failure investigation discussions for issues related to Franchise product quality.
• Team development, mentoring and training team members.
  
  

• BSc in Engineering or Practical Engineering with Qualification in Quality Assurance (CQE, CQM or CQA).
• At least 5 years of experience as a quality leader in a WW manufacturing organization (preferably, Medical Devices Industry)
• Practical knowledge of ISO13485, Experience in the Medical Device industry or medical field
• Demonstrated knowledge of manufacturing principles and practices, and procedures
• Demonstrated knowledge of Statistical Analysis Tools
• Must be a self-starter/able to think outside the box, challenge the norm and drive change.
• Ability to collaborate and build strong partnerships internally/externally with customer focus.
• Must have excellent communication, interpersonal and presentation skills (Also in English)
• Significant teamwork and leadership skills
• Demonstrate project management skills with strong results orientation.
• Self-confidence and integrity
• Builds relationships based on respect, listens to and incorporates diverse points of view.