🥉 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 (5 years)
- 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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