Quality Coordinator EMEA.

☞ Johnson & Johnson

Vue: 155

Jour de mise à jour: 16-11-2025

Localisation: Brussels Brussels Capital

Catégorie: Assurance Qualité / Contrôle Qualité

Industrie: Hospital & Health Care Medical Devices Pharmaceuticals

Type d’emploi: Full-time

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le contenu du travail

Quality Coordinator EMEA in the European Headquarters (EHQ) Diegem, Belgium / Medical Devices

Job Description

Biosense Webster, Inc., part of Johnson & Johnson Medical Devices Companies, is recruiting for a Quality Coordinator EMEA to be based in the European Headquarters (EHQ) in Diegem, Belgium.

Atrial fibrillation (AFIB) is a quivering or irregular heartbeat (arrhythmia) that can lead to blood clots, stroke, heart failure and other heart-related complications. 20 million people around the world suffer from AFIB each year. Biosense Webster, Inc. (BWI) is the global leader in the science of diagnosing and treating heart rhythm disorders. The company established its leadership in electrophysiology with the development of the first real-time, 3D cardiac mapping and navigation technology, as well as the first electrophysiology catheter. The introduction of the company’s CARTO® 3 System in 2009 revolutionized 3D mapping technology by increasing the accuracy, speed, and efficiency of the cardiac ablation procedure. Biosense Webster is part of the Cardiovascular and Specialty Solutions Group of Medical Device sector of Johnson and Johnson.

This position will be responsible for maintaining Quality and Compliance at EHQ.

Key Responsibilities
  • Acts as OUS quality hold coordinator
  • Supports EMEA field action execution
  • Ensures training objectives are met for BWI EMEA
  • Possesses understanding of European medical devices regulations and keeps abreast of changes in the regulatory environment
  • Develops, prepares, and analyzes queries for complaints, as required.
  • Investigates and develops solutions to procedure and process related issues
  • Participates on project teams to improve processes within the European HQ.
  • Executes inspection of the returned products
  • Ensuring personal and company compliance with all National and company regulations, policies and procedures.

Qualifications

Qualifications

Education

At the minimum BS/BA degree in business or science, with a QA environment experience preferred.

Required Skills

English proficiency oral and written. Must have adequate computer skills to evaluate trending data, complete regulatory reports, and provide written correspondence to internal and external customers including regulatory bodies as appropriate, including:
  • Communication - written & verbal in a clear, concise & effective manner.
  • Interpersonal skills - interact with all levels, personalities, cultures & disciplines of organization to produce required results.
  • Investigative & analytical - to establish possible options for action.
  • Results oriented - in a fast-paced environment.
  • Leadership skills.

Other

This role is based in Diegem, Belgium

Travel: occasional travel might be required

Johnson & Johnson is an Affirmative Action and Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, age, national origin, or protected veteran status and will not be discriminated against on the basis of disability.

Primary Location

Belgium-Brussels-Capital Region-Diegem-

Organization

Johnson & Johnson Medical NV (7546)

Job Function

Quality

Requisition ID

2105977139W

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Date limite: 31-12-2025

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