Global MDRIM & Documentation Project Manager

Johnson & Johnson MedTech

Diegem

Hybride

EUR 70 000 - 110 000

Plein temps

Il y a 4 jours
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Résumé du poste

Johnson & Johnson seeks a Project Manager for MDRIM & Document Management to lead regulatory information management and document workflows across a multinational setting. This hybrid role emphasizes on‑time delivery, compliance, and cross‑functional collaboration within QARA International.

You will drive documentation standards, manage milestones, and liaise with Regulatory Affairs, Quality, R&D, and Manufacturing to improve processes and readiness for inspections.

Qualifications

  • Bachelor’s degree required in Life Sciences, Engineering, Quality, Regulatory Affairs, or a related discipline.
  • Master’s degree preferred.
  • 6–8 years of project management, quality, regulatory, or document management experience in a regulated industry.

Responsabilités

  • Lead MDRIM and document management projects from initiation to completion.
  • Coordinate cross‑functional stakeholders to align documentation requirements.
  • Plan, track, and report milestones, risks, and dependencies.
  • Ensure processes comply with global regulations and quality standards.
  • Drive continuous improvement of MDRIM workflows.
  • Maintain project documentation, dashboards, and metrics.
  • Facilitate governance meetings and stakeholder communications.

Connaissances

Project management
Regulatory affairs
Quality systems
Documentation management
Cross-functional collaboration

Formation

Bachelor’s degree in Life Sciences/Engineering/Quality/Regulatory Affairs
Master’s degree preferred

Description du poste

Johnson & Johnson seeks a Project Manager for MDRIM & Document Management to lead regulatory information management and document workflows across a multinational setting. This hybrid role emphasizes on‑time delivery, compliance, and cross‑functional collaboration within QARA International.

You will drive documentation standards, manage milestones, and liaise with Regulatory Affairs, Quality, R&D, and Manufacturing to improve processes and readiness for inspections.

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