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Regulatory Affairs Specialist

hace 2 meses

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

Zimmer Biomet is a global medical technology leader with a nearly 100-year history of innovation. Our mission is to enhance patients' mobility and quality of life through our products and technologies.

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
  • Conduct regulatory research and analysis to stay up-to-date on changing regulations
  • Prepare and submit regulatory documents, including 510(k) and PMA submissions
  • Develop and maintain regulatory training programs for employees
What You'll Bring
  • Strong knowledge of regulatory requirements for medical devices
  • Excellent communication and collaboration skills
  • Ability to work in a fast-paced environment and prioritize multiple tasks
  • Strong analytical and problem-solving skills
  • Experience with regulatory software and systems
What We Offer

At Zimmer Biomet, we offer a competitive total rewards package, including a comprehensive benefits program, flexible working environment, and opportunities for professional growth and development. We are committed to creating an inclusive and diverse work environment where every team member feels valued and empowered to contribute their best work.

We are an equal opportunity employer and welcome applications from diverse candidates. EOE/M/F/Vet/Disability