Regulatory Affairs Specialist

hace 1 semana


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 a 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 safe and effective use of our products.

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 and maintain regulatory documentation and records
  • Stay up-to-date with changing regulatory requirements and industry trends
What You'll Bring
  • Strong knowledge of regulatory requirements and industry standards
  • 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 documentation and record-keeping
What We Offer
  • A dynamic and supportive work environment
  • Opportunities for professional growth and development
  • A competitive total rewards package
  • A commitment to diversity, equity, and inclusion
  • A culture of recognition and performance awards

Zimmer Biomet is an equal opportunity employer and welcomes applications from diverse candidates. We are committed to creating an inclusive environment where every team member feels valued, respected, and empowered to contribute their best work.



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