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Regulatory Affairs Specialist

hace 1 mes

Bogotá, Bogotá D.E., Colombia Zimmer Biomet A tiempo completo
About Zimmer Biomet

Zimmer Biomet is a global medical technology leader with a rich history of innovation and commitment to enhancing patient mobility.

Job Summary

We are seeking a highly skilled Regulatory Affairs Specialist to join our team. As a key member of our regulatory team, you will play a critical role in ensuring compliance with regulatory requirements and ensuring the quality and safety of our medical devices.

Key Responsibilities
  • Develop and implement regulatory strategies to ensure compliance with global regulations
  • Collaborate with cross-functional teams to ensure regulatory requirements are met
  • Provide regulatory guidance and support to product development teams
  • Manage regulatory submissions and interactions with regulatory agencies
  • Stay up-to-date with changing regulatory requirements and industry trends
What You Can Expect

As a Regulatory Affairs Specialist at Zimmer Biomet, you can expect a dynamic and challenging work environment with opportunities for growth and development. You will be part of a talented team that is passionate about making a difference in the lives of patients around the world.

How You Will Make an Impact

You will have a direct impact on the quality and safety of our medical devices, ensuring that they meet the highest regulatory standards. Your expertise will help us to stay ahead of the competition and maintain our position as a leader in the medical technology industry.

What Sets Us Apart

Zimmer Biomet is committed to creating an environment where every team member feels inspired, invested, cared for, valued, and has a strong sense of belonging. We offer a range of benefits and programs to support your career development and well-being, including flexible working arrangements, employee resource groups, and a culture of recognition and performance awards.

Your Experience

We are looking for a highly skilled Regulatory Affairs Specialist with a strong background in regulatory affairs and a passion for ensuring the quality and safety of medical devices. You will have a bachelor's degree in a relevant field and at least 3 years of experience in regulatory affairs.

Travel Expectations

This role may require occasional travel to regulatory agency meetings and industry conferences.

Zimmer Biomet is an equal opportunities employer and welcomes applications from diverse candidates. EOE/M/F/Vet/Disability