Senior Expert Regulatory Affairs (m/f/x)

Zeiss Group

Aalen, Germany
Strong experience in regulatory affairs
Knowledge of eu mdr and uk mdr
Experience with fda requirements
As a leading manufacturer of ophthalmic lenses, we help people around the world achieve a clearer vision

Job Summary

  • As a leading manufacturer of ophthalmic lenses, we help people around the world achieve a clearer vision.
  • You will oversee preparation and submission of regulatory documents to authorities.
  • Become part of our team and shape a future in which clear vision and professional success go hand in hand.

Matching Summary

As a leading manufacturer of ophthalmic lenses, we help people around the world achieve a clearer vision.

Skills & Requirements

Must-have

  • Strong experience in regulatory affairs
  • Knowledge of EU MDR and UK MDR
  • Experience with FDA requirements

Nice-to-have

  • Strong analytical and problem-solving skills
  • Excellent communication and negotiation skills
  • Fluency in English and German

Key Requirements

  • BS/MSc in Life Sciences or Engineering
  • Experience in medical devices or pharma
  • Certifications in ISO 13485 or MDSAP

Work Rights

Not specified

Tailored Resume

Cover Letter