Quality and Regulatory Affairs Specialist

1 dzień temu


Warszawa, Mazovia, Polska Zimmer Biomet Pełny etat
About the Role

Zimmer Biomet is a global medical technology leader, and we're committed to enhancing patient mobility and quality of life. As a Quality and Regulatory Affairs Associate, you'll play a critical role in ensuring our products meet the highest standards of quality and regulatory compliance.

Key Responsibilities
  • Support the implementation, maintenance, and control of a quality management system according to international standards and corporate guidelines.
  • Assure effective, consistent, and reliable forward of information in terms of product surveillance in assigned regions and local markets.
  • Ensure surveillance and forward of information concerning changes and/or new upcoming local legal requirements to assure the continuity of Zimmer Biomet's business.
Requirements
  • Bachelor's degree in engineering, business, political science, or equivalent experience.
  • First experience in registration activities and/or quality assurance is an asset.
  • Strong organizational, follow-up, and time management skills.
  • Ability to work independently and under pressure.
  • Experience with Windows Office Software is required; SAP is an asset.
  • English fluency is required; Arabic and French are an asset.
What We Offer

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 flexible working environment, competitive total rewards, wellness incentives, and a culture of recognition and performance awards.



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