Quality and Regulatory Affairs Specialist
3 tygodni temu
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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