Chargement en cours

Medical Devices Associate

PARIS, 75
il y a 13 heures

Your Mission

As a Medical Device Associate , you will support regulatory and quality activities for medical devices, ensuring compliance with international regulations and quality standards while contributing to a wide range of client projects.

Key Responsibilities

  • Support regulatory affairs activities for medical devices across international markets.
  • Prepare, maintain, and review quality documentation including SOPs, working instructions, and templates.
  • Contribute to the preparation and maintenance of Technical Documentation, STEDs, and Declarations of Conformity.
  • Review Labelling and advertising documents.
  • Support CAPA management, non-conformity investigations, and quality improvement activities.
  • Participate in internal and external audits, including ISO 13485-related activities.
  • Support regulatory registration and approval activities, including EU and FDA-related projects.
  • Monitor regulatory developments and assess their impact on projects and processes.
  • Contribute to KPI tracking and reporting through PLG systems and tools
  • Collaborate with cross-functional and international teams to deliver high-quality client services.

Profile

  • Bachelor's degree in Life Sciences, Pharmacy, Biomedical Engineering, Regulatory Affairs, or a related scientific field.
  • Experience in Medical Device Regulatory Affairs and/or Quality Assurance.
  • Knowledge of MDR, IVDR, ISO 13485, Technical Documentation, CAPA, and quality systems.
  • Excellent organizational and communication skills.
  • Fluent in French and English.
  • Proactive, detail-oriented, and able to work in an international environment.

Why Join PLG?

  • Work on international and innovative medical device projects.
  • Collaborate with regulatory and quality experts worldwide.
  • Benefit from continuous learning and professional growth opportunities.
  • Join a dynamic company committed to improving patient access to safe healthcare solutions.

Ready to make an impact? Join PLG and help shape the future of medical device compliance.

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Entreprise
ProductLife Group
Plateforme de publication
WHATJOBS
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