Regulatory Affairs professionals gezocht, medical devices

South Holland
Jan 04, 2021
Feb 03, 2021
Debie Biharie
Organization Type
Contract Type
Full Time

Heb jij het volgende profiel solliciteer dan nu!

  • Je hebt een master in Biology/ Biomedische studies of life sciences
  • Minimaal 2 tot 10 jaar ervaring in regulatory affairs of quality assurance in medical devices
  • Goed op de hoogte van relevante internationale regelgeving op het gebied van IVD's en eventuele wijzigen in deze met betrekking tot ISO 13485, Europese IVD directive (98/79/EC), Europese IVD regulaties (EU 2017/746)
  • Kennis van Chinese FDA en USA FDA (21 CFR820)
  • Je hebt voldoende kennis in genetics
  • Je spreekt en schrijft vloeiend Engels

  • Soliciteer nu en contacteer mij direct! Mocht je zelf niet beschikbaar zijn deel deze vacature en help iemand in jouw netwerk.
  • Debie Biharie
    Consultant/ Headhunter Pharma Regulatory Affairs Netherlands
    NonStop Pharma
  • BE: +32 289 198 99
  • NL: +31 207 091 070
  • LU: +35 220 204 215
  • Internal Extension: 3394
  • Email:

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