Doc Control Supervisor
J&J Family of Companies
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:**
Customer/Commercial Quality
**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 the best talent for a Doc Control Supervisor role, to join our team located in Yokneam, Israel.**
**Purpose:** The chosen candidate will be responsible for the revision and change control of production files and controlled documents..
Leads the Document Control activities to ensure company compliance with documentation procedures and to ensure proper documentation control.
Direct responsibility for Documentation Experts
**You will be responsible for** **:**
+ Revision and change control of HTC production files (DMRs) and customer support documents
+ Handling Document Approval (DAP) in HTC PLM System
+ Ensure High Quality of HTC Revision and Change Control
+ Leads ECO process continuous improvement
+ Leads JDE Coordinator responsibilities
+ Team Development
**Qualifications and Requirements:**
+ BA or BSc degree.
+ Experience reviewing technical documents (in English and Hebrew).
+ Experience in a documentation or engineering department.
+ Experience working with Agile
+ Experience in Medical Device industry or medical fields - advantage
+ Good understanding of technical processes
+ Microsoft Office
+ Good sense of urgency, problem solving, good communication skills, both verbal and written
+ Good English skills
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