We are a global leader in the design, manufacture, and distribution of ophthalmic lenses, frames, and sunglasses. We offer our industry stakeholders in over 150 countries access to a global platform of high-quality vision care products and iconic brands. Join our global community of over 190,000 dedicated employees around the world in driving the transformation of the eyewear and eyecare industry.
Requirements
- Support the implementation, maintenance, and improvement of global Quality Management Systems (QMS) in compliance with ISO 9001, ISO 13485 with MDSAP standards.
- Contribute to ensuring product compliance with international regulations, including USA FDA, EU MDR 2017/745, and EU PPE 2016/425.
- Participate in the preparation, coordination, and follow-up of internal and external audits to ensure audit readiness.
- Collaborate with cross-functional teams across design, production, and distribution to maintain regulatory and quality compliance.
- Assist in the development, review, and maintenance of technical files and regulatory documentation.
- Maintain accurate and traceable records to support compliance and inspection activities.
- Contribute to quality and regulatory projects throughout the entire product lifecycle.
- Support standardization and continuous improvement initiatives across multiple international sites.
- Facilitate communication and alignment on Quality Assurance and Regulatory Affairs (QA/RA) processes between global departments.
- Apply knowledge of international standards and regulatory frameworks to real projects and business operations.
Benefits
- Hands-on experience with global quality systems and regulatory compliance across a diverse product portfolio
- Gain in-depth knowledge of international standards and regulations such as ISO 9001 and ISO 13485 with MDSAP, USA FDA and EU MDR 2017/745, EU PPE 2016/425
- Contribute to Quality Assurance & Regulatory Affairs projects across the product lifecycle
- Opportunity to grow into a Quality Assurance & Regulatory Affairs Intern role