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Quality Assurance Labelling Manager - EMEA - Medical Devices

  • Michael Page
  • Oost-Vlaanderen
  • Lead the Quality Assurance Labelling teams, ensuring continuous improvement and regulatory...
  • Contribute to the strategic planning and direction of the Quality Assurance department.
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Michael Page

Quality Assurance Labelling Manager - EMEA - Medical Devices

Voltijds
Staat 9 dagen op Jobat.be

Our client is a large multinational medical devices company leader in the life science industry with over 10,000 employees worldwide. The company is renowned for innovative solutions that contribute to enhancing health and well-being globally.

Quality Assurance Labelling Manager - EMEA - Medical Devices

Functieomschrijving

As a successful Quality Assurance Labelling Manager - Medical Device company you will have the following responsibilities:

Leadership activities:


  • Lead the Quality Assurance Labelling teams, ensuring continuous improvement and regulatory compliance.

  • Contribute to the strategic planning and direction of the Quality Assurance department.

  • Oversee the training of staff in labelling procedures and regulatory requirements.

  • Develop and implement labelling procedures, quality processes and quality control measures in compliance with ISO 13485.

  • Work collaboratively with other departments to streamline labelling processes (Regulatory Affairs, supply chains, Business Units...).




Quality Assurance:


  • Be responsible for labeling activities requests from the initiation until the approval.

  • Ensure all labelling activities adhere to international regulatory standards and compliance ( ISO 13485, GDP, GMP, MDR, and IVDR regulations).

  • Handle EMEA products complaints, CAPAs and deviations linked to labelling activities.

  • Conduct & Coordinate regular audits and reviews to ensure labelling accuracy.

  • Manage labelling documentation, maintaining records of all quality assurance activities.

Profiel

As a successful Quality Assurance Labelling Manager - Medical Device company you will have the following profiles:


  • A degree in Life Sciences or a related field.

  • Experience in ISO 13485, GDP, GMP, and European Regulations.

  • Experience in Quality Assurance, QMS and internal audits.

  • Knowledge of international regulatory standards related to product labelling.

  • Strong leadership skills with an ability to motivate and develop a team.

  • Excellent communication and interpersonal skills.

  • Fluent in Dutch & English, French being plus.

Aanbod

As a successful Quality Assurance Labelling Manager - Medical Device company you will have:


  • An competitive fix salary including a bonus and a package of extra legal benefits

  • The chance to join a global organization with multiple growing opportunities.

  • The possibility to join a positive multicultural team contributing to the diversity and well-being of individuals all around the world.




If you are passionate about quality assurance and looking to take the next step in your career, we encourage you to apply for this exciting opportunity.

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