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Regulatory Affairs Specialist

2 meses atrás

São Paulo, São Paulo, Brasil Zimmer Biomet Tempo inteiro
Job Title: Regulatory Affairs Manager

Zimmer Biomet is seeking a highly skilled Regulatory Affairs Manager to join our team in Brazil. As a key member of our regulatory team, you will be responsible for managing all facets of regulatory and quality functions to ensure compliance with local and international regulations.

Key Responsibilities:
  • Develop and implement regulatory strategies to ensure compliance with local and international regulations.
  • Manage the preparation and submission of regulatory documents to government agencies.
  • Collaborate with cross-functional teams to ensure regulatory compliance throughout the product lifecycle.
  • Provide guidance and training to colleagues on regulatory requirements and best practices.
  • Stay up-to-date with changes in regulations and industry trends to ensure Zimmer Biomet remains compliant and competitive.
Requirements:
  • Bachelor's degree in a life science or related field.
  • Advanced English language skills.
  • Minimum 5 years of experience in regulatory affairs, including preparation of submissions to government agencies and quality management systems.
  • Experience in the medical device industry, biologics, and/or combination products is preferred.
What We Offer:
  • A dynamic and collaborative work environment.
  • Opportunities for professional growth and development.
  • A competitive salary and benefits package.
  • The chance to work with a global leader in the medical technology industry.

Zimmer Biomet is an equal opportunities employer and welcomes applications from diverse candidates. We are committed to creating an inclusive and respectful work environment that values diversity and promotes equal opportunities for all employees.