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Quality Systems Team Leader

Johnson & Johnson MedTech · District de Haïfa

חדש
🇬🇧 English
CAPA governance Quality Agreements cGMP training Document and records management ISO standards Quality System Regulation Data analysis Statistical tools

תיאור המשרה

About the role

Johnson & Johnson MedTech Cardiovascular is seeking a Quality Systems Team Leader to lead key site Quality System processes and a multidisciplinary team. The role focuses on strengthening compliance, improving quality performance and partnering with local and global functions to ensure effective, sustainable processes.

Key responsibilities

  • Lead and continuously improve site Quality System processes, including CAPA, Quality Agreements, training, the Quality Manual, and document/records management.
  • Manage CAPA governance, investigations, implementation plans, effectiveness checks, metrics, escalation and timely closure.
  • Ensure Quality Agreements are aligned with company processes and supported by appropriate controls.
  • Lead quality and cGMP training activities, coach employees and process owners on Quality System expectations.
  • Maintain and improve Quality System procedures in line with regulations, standards and company requirements.
  • Provide leadership for Enterprise Retention Schedule, Legal Hold preservation, and Vital Records inventory compliance.
  • Oversee physical‑records lifecycle, including active onsite records, transfer, off‑site archiving and archive‑box monitoring.
  • Partner with local and global stakeholders to resolve quality challenges, identify improvement opportunities and support audit readiness.
  • Lead, coach and develop the Quality Systems team, building capability and accountability.

Required profile

  • Bachelor’s degree or higher in engineering, science, quality, statistics or a related field.
  • 2‑4 years experience leading quality assurance or Quality System activities in a regulated environment.
  • 5‑7 years working knowledge of medical‑device or pharmaceutical Quality System requirements, including ISO standards and Quality System Regulation.
  • Experience interacting with regulatory authorities, notified bodies or external auditors.
  • Demonstrated leadership of people, projects or cross‑functional initiatives.
  • Strong written and verbal English communication skills.

Required skills

  • CAPA governance and implementation.
  • Quality Agreements development and control.
  • cGMP training design and delivery.
  • Document and records management, including electronic and physical records.
  • Knowledge of ISO standards and Quality System Regulation requirements.
  • Data analysis and statistical tools for quality performance monitoring.

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Johnson & Johnson MedTech

District de Haïfa