Quality LCM Manager

Posted Yesterday
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Yokneam
In-Office
Senior level
Healthtech • Pharmaceutical • Manufacturing
The Role
The Quality LCM Manager at Johnson & Johnson is responsible for managing quality assurance activities, product lifecycle management, and team development within Cardiovascular solutions.
Summary Generated by Built In

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 Assurance

Job Category:

People Leader

All Job Posting Locations:

Yokneam, Haifa District, Israel

Job Description:

About Johnson & Johnson MedTech 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 the best talent for a Quality LCM Manager role, to join our team located in Yokneam, Israel.
Purpose: The Manager Quality LCM Responsible for plan, manages and coordinates quality assurance activities designed to ensure effective new product Introduction, lifecycle management, product quality and supplier management.

You will be responsible for:

  • 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 quality improvement opportunities, continuous improvement, and strives to customer satisfaction

  • Lead transferring new product, major product or process change from development to production until the product/process

  • Lead the quality LCM activities such as calibration, PM, QC & Final release, non-conforming management etc.

  • Promotes DFx methodology within the operations, suppliers and Development teams

  • Manage Process validation/ Verification activities

  • Team development, Mentor and trains team members.

Qualifications and Requirements:

  • 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.

#LI-AB6

#LI-Hybrid



Required Skills:



Preferred Skills:

Compliance Management, Corrective and Preventive Action (CAPA), Cross-Functional Collaboration, Developing Others, Fact-Based Decision Making, Give Feedback, Good Manufacturing Practices (GMP), Inclusive Leadership, ISO 9001, Leadership, Quality Control (QC), Quality Management Systems (QMS), Quality Standards, Quality Validation, Risk Assessments, Standard Operating Procedure (SOP), Tactical Thinking, Team Management

Top Skills

Corrective And Preventive Action (Capa)
Good Manufacturing Practices (Gmp)
Iso 13485
Quality Management Systems (Qms)
Quality Standards
Statistical Analysis Tools
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The Company
HQ: New Brunswick, NJ
143,612 Employees
Year Founded: 1886

What We Do

Profound Change Requires Boldness.

Johnson & Johnson is the largest and most broadly based healthcare company in the world. We’re producing life-changing breakthroughs every day, and have been for the last 130 years.

The combination of new technologies and your expertise enables amazing things to happen. Teams from J&J’s consumer business are creating digital tools to help people track the health of their skin. Those working in medical devices are 3-D printing artificial joints personalized for each patient, while researchers in pharmaceuticals use AI to discover lifesaving drugs. Imagine what the rest of our team of 134,000 people at 260 companies in more than 60 countries across the world is accomplishing. We redefine what it means to be a big company in today’s world.

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