🥉 To be considered for this position, the following skills have to be obvious on your education / experiences:
Master degree (Scientific, Biomedical Engineer or equivalent) with a specialization in Regulatory Affairs (UTC, ISIFC, etc.)
You know of the ISO 13485 (school or professional experience)
You know the Medical Device Regulation (2017/745)
You speak fluently French & English
You have a strong work ethic & daily act with integrity, honesty and fairness
You are definitely a thoughtful team player, looking to make your colleagues successful.
🥈 In addition, here are some important basics to succeed in this position:
Previous experience in Quality and/or Regulatory
You are self-driven and definitely able to multi-task
You have writing skills (both in French & English)
You have a strong bias for action, and get things done, even if you don’t fully understand everything
You have Strong interest in the innovation and health ecosystem
You are IT agile (we use Notions, Slack, Drive, etc.) as daily tools
🥇 The bonus skills that would definitely make us pick you:
You know the FDA regulation
You have writing skills (both in French & English)
Low-ego & High-energy, you are definitely resilient
You are a Do-er / pb-solver, enjoy overcoming barriers and helping the team to win
You like this ad, and think this is very like you 😊
It is OK to apply without meeting all the 2nd and 3nd paragraph skills: just honestly tell us why you think you can be THE one.
General information
💰 Salary
👍 Benefits
📍 Remote work & Location
✅ Why us?
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