Quality and Regulatory Affairs Specialist

3 tygodni temu


Warszawa, Mazovia, Polska Zimmer Biomet Pełny etat

At Zimmer Biomet, we are committed to delivering innovative medical solutions that enhance patient mobility and quality of life. As a Quality and Regulatory Affairs Associate, you will play a critical role in ensuring the compliance of our products with local regulations and standards.

Key Responsibilities:

  • Support the implementation and maintenance of a quality management system in accordance with international standards and corporate guidelines.
  • Ensure effective communication with local authorities and stakeholders to facilitate product registration and surveillance.
  • Monitor and report on changes to local regulations and standards to ensure Zimmer Biomet's business continuity.

Requirements:

  • Bachelor's degree in engineering, business, or a related field.
  • 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.

Additional Requirements:

  • Proficiency in Windows Office Software and SAP is an asset.
  • English fluency is required, with Arabic and French being an asset.

Zimmer Biomet is an equal opportunity employer and welcomes applications from diverse candidates.



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