Quality Compliance & Regulatory Internship

If you’ve worn a pair of glasses, we’ve already met.

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 [such as the Essilor brand, with Varilux, Crizal, Eyezen, Stellest and Transitions], iconic brands that consumers love [such as Ray-Ban, Oakley, Persol, Oliver Peoples, Vogue Eyewear and Costa], as well as a network that offers consumers high-quality vision care and best-in-class shopping experiences [such as Sunglass Hut, LensCrafters, Salmoiraghi & Viganò and the GrandVision network], and leading e-commerce platforms.

Join our global community of over 190,000 dedicated employees around the world in driving the transformation of the eyewear and eyecare industry.
Discover more by following us on LinkedIn!

Your #FutureInSight with EssilorLuxottica

Are you willing to pioneer new frontiers, foster inclusivity and collaboration, embrace agility, ignite passion, and make a positive impact on the world? 

Join us in redefining the boundaries of what’s possible!

Your role 

We are looking for a motivated, curious and enterprising candidate to join us at our Operations HQ in Agordo (BL, Italy).
As Quality Compliance & Regulatory Intern you will support the quality team in different areas.

Main responsibilities: 

• Coordinate the Extended Product Responsibility activity according to the EPR Requirements (packaging, WEEE, batteries, textile), including labelling and Plastic Tax topics according to the new requirement in place and that will be released in the world
• Update the training materials on Dangerous Goods 
• Support the quality compliance activities related to “SPECIAL PROJECTS” 
• Management of issues related to medical device and biocompatibility topics according to medical devices quality compliance point of view.
• Validation and certification of medical devices and software systems, according to medical device requirements.
• Optimization and standardization of quality approach in retails and eCommerce channels.

Main Requirements:

• You are an excellent performer with a proven excellence in academic and professional life.
• You have a Master's degree in Engineering
• You have a passion for the quality system
• You have a great knowledge of Office package (Excel, Power Point,..)
• You have some knowledge about Biomedical / Medical Device Regulation
• Fluent in English, both written and spoken
• You have at least 0-1 years of experience

Our Diversity, Equity and Inclusion commitment

We are committed to creating an inclusive environment for all employees. We celebrate diversity and provide equal opportunities to all, regardless of race, gender, ethnicity, religion, disability, sexual orientation, or any other characteristic that makes us unique.

We welcome applications from all individuals regardless of their ages, backgrounds, gender, sexual orientation, political affiliations, personal beliefs, or religions. This includes those registered in targeted employment programs under Italian Law 68/1999, in accordance with Article 15 of Stat. Lav and Legislative Decrees 215/03 and 216/03.