Position: Entry level

Job type: Full-time

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Job content

  • Mid-sized organisation
  • Young and dynamic team
About Our Client

Our client is a mid-sized organisation developing medical devices.

Job Description
  • Support R&D project and improvement project from quality perspective specially for risk management process and any quality impact on design process.
  • Review of the sterilization documents of the finished sterile products (legal manufacturer) as part of the release of the products.
  • Internal expert of biocompatibility and connected devices.
  • Internal expert of risk management.
  • Participate to the creation of SOP of the quality system related quality management.
  • Ensure good cooperation and communication within the team and with other teams and departments.
  • Continuously look for improvements in working procedures within the team and across other departments, if relevant.
  • Ensure a high level of quality of work within the team.
  • Support and improve quality system management in compliance with applicable requirements (ISO 9001, ISO 13485, QSR 21 CFR 820, …).
  • Promote continuous improvement process (CAPA and Change management).
  • Participate to third parties audits (Bodies notified, authorities, ISO 13485, FDA, etc).
The Successful Applicant
  • Quality Engineer or Technician degree
  • 1 to 3 years of experience in Quality Assurance
  • ISO 13485, MDD / MDR and 21 CFR part 820
  • Biocompatibility
  • Risk management
  • Release sterilization document
  • Conscientious, diplomatic and rigorous
  • Fluent in French and English
What’s On Offer

Great opportunity to join a dynamic and multi-tasking environment.

Contact: Julie Ardouin

Quote job ref: JN-072021-2947917

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Deadline: 10-05-2024

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