MASTER DI ALTA FORMAZIONE IN QUALITY ASSURANCE & REGULATORY AFFAIRS DI DISPOSITIVI MEDICI E IVD RICONOSCIUTO AICQ-SICEV

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Qualifications:

Bachelor's degree in a relevant field such as life sciences or engineering., Experience in quality assurance and regulatory affairs for medical devices and IVDs., Strong understanding of compliance standards and regulations., Excellent analytical and communication skills..

Key responsibilities:

  • Develop and implement quality assurance processes for medical devices.
  • Ensure compliance with regulatory requirements and standards.
  • Conduct audits and assessments of quality systems.
  • Collaborate with cross-functional teams to improve product quality.

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GRUPPO MIDI http://www.gruppomidi.it
2 - 10 Employees
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