Medical Device Compliance Specialist

3 weeks ago


Temecula, California, United States Collabera Full time
Job Role

We are seeking an experienced Senior Regulatory Affairs Specialist to join our team and contribute to the development of regulatory affairs processes. In this role, you will work closely with internal and external stakeholders to implement regulatory strategies, manage product registrations, and ensure compliance with regulatory requirements.

Key Requirements
  • Bachelor's degree in a relevant field (e.g., life sciences, law).
  • 1-3 years of experience in medical device regulatory affairs.
  • Strong knowledge of EU MDR, US FDA regulations, and regulatory change assessment.
  • Excellent communication and project management skills.

The estimated annual salary for this role is $130,000, based on location and experience. We offer a comprehensive benefits package and opportunities for professional growth and development.



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