Regulatory Affairs Specialist DM

il y a 5 heures


Paris, Île-de-France NEO2 Temps plein
Join NEO2 as a Regulatory Affairs Specialist DM

NEO2 is seeking a highly skilled Regulatory Affairs Specialist DM to join our team. As a Regulatory Affairs Specialist DM, you will be responsible for ensuring compliance with regulatory requirements and developing strategies to mitigate risks.

Main Responsibilities:

  • Obtain and maintain CE marking
  • Manage technical documentation
  • Coordinate with notified bodies
  • Monitor regulatory changes related to CE marking
  • Provide internal support on regulatory aspects

About NEO2:

NEO2 is a leading company in the medical devices industry. We are committed to providing innovative solutions that meet the needs of our customers. As a Regulatory Affairs Specialist DM, you will be part of a dynamic team that is passionate about delivering high-quality products.

What We Offer:

  • A challenging and rewarding role with opportunities for growth and development
  • A collaborative and supportive work environment
  • A competitive salary and benefits package

Requirements:

  • Strong knowledge of regulatory requirements related to CE marking
  • Excellent communication and project management skills
  • Ability to work independently and as part of a team

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