Product Registration and Regulatory Lead

4 hours ago


Gothenburg, Västra Götaland, Sweden Moveup Consulting AB Full time

XVIVO is a rapidly growing medical technology company that develops innovative solutions to extend the life of organs for transplant patients. As a Regulatory Affairs Manager, you will play a critical role in shaping the company's future.

Responsibilities

The key responsibilities of this position include:

  • Ensuring compliance with regulatory requirements for XVIVO's products in various markets.
  • Liaising with stakeholders to develop and implement regulatory strategies.
  • Managing regulatory affairs for new product launches.
Requirements

The ideal candidate will have:

  • A bachelor's degree in a relevant field such as Science, Engineering, or Medicine.
  • Professional experience in Regulatory Affairs, with a strong understanding of quality management systems and medical device regulations.
  • Excellent communication and project management skills.
Why Join Us

XVIVO offers a competitive salary package, a dynamic and supportive work environment, and opportunities for professional growth and development.



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