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Auditor - Technical File Reviewer

EPM Scientific

Remote

EUR 80.000 - 100.000

Vollzeit

Heute
Sei unter den ersten Bewerbenden

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Zusammenfassung

A reputed certification company in Germany is seeking an Auditor for a remote position to conduct technical file reviews and audits of active medical devices. The role involves ensuring compliance with international standards and addressing any product safety issues. Candidates must hold a relevant degree and have experience in technical file reviews. Fluency in German is essential for this role. This position offers the chance to work in a critical sector with international operations.

Qualifikationen

  • Experience in active medical device technical file reviews and testing/inspection.
  • Familiarity with med tech and diagnostics products.
  • Ability to conduct conformity assessments.

Aufgaben

  • Participate in reviews of technical files related to active medical devices.
  • Conduct conformity assessments to international/regional standards.
  • Ensure technical files comply with standards and assess product safety.

Kenntnisse

Familiarity with active medical device products
Fluent in German language
Communication skills
Project management skills

Ausbildung

Bachelor's, Master's or Doctoral degree in Biology, Chemistry, Pharmacy, Medicine, Agriculture, Veterinary Medicine
Jobbeschreibung

Our client is an established notified body with international operations. They test, audit, inspect and advise medical technology clients.

They are looking to add an Auditor to the team in Germany conducted technical file reviews and audits of active medical devices.

The certification company have offices in Germany and internationally, however this is a remote position.

Duties
  • As Auditor, you will participate in reviews of technical files related to domestic and international laws and regulations related to active medical device. This will be across med tech and diagnostics products
  • You will conduct conformity assessment to international / regional standards (ISO13485 etc.) and technical document evaluations
  • The aim of the position is to ensure technical files are compiled in accordance with standards and whether there are any problems with product safety, documents / files
Qualifications
  • You will need familiarity with active medical device products
  • Have either a Bachelor's, Master's or Doctoral degree (Biology, Chemistry, Pharmacy, Medicine, Agriculture, Veterinary Medicine, etc.)
  • Experience in active medical device technical file reviews and testing / inspection
  • Fluent in German language (written and spoken)
  • Communication and project management skills
Desired Skills and Experience

audit, technical files, active medical devices, German, notified body

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