WHO WE ARE We are EssilorLuxottica, a global leader in the design, manufacture and distribution of ophthalmic lenses, frames and sunglasses. The Company brings together the complementary expertise of two industry pioneers, one in advanced lens technologies and the other in the craftsmanship of iconic eyewear, to create a vertically integrated business that is uniquely positioned to address the world's evolving vision needs and the global demand of a growing eyewear industry. With over 180,000 dedicated employees in 150 countries driving our iconic brands, our people are creative, entrepreneurial and celebrated for their unique perspectives and individuality. Committed to vision, we enable people to "see more and be more" thanks to our innovative designs and lens technologies, exceptional quality and cutting-edge processing methods. Every day we impact the lives of millions by changing the way people see the world. ENVISION YOUR FUTURE JOB
We are looking for a motivated, curious and enterprising candidate to join us at our Operations HQ in Agordo (BL, Italy).
As Quality Compliance Medical Device intern you will understand deeply the regulations governing the smart eyewear industry and develop practical skills in the field of quality compliance and regulation, a profound level of understanding of the development of innovative eyewear models and their release into the market, with commitment to adhere to procedures and instructions of the Quality System.
Here are some responsibilities you will have:
Study and understand international, test standard and local regulations related to smart eyewear, including EMC, safety, battery, BT and medical device requirements. Monitor regulatory and legislative updates relevant to the industry. Assist in preparing compliance documentation, including reports, instruction for use and declarations of conformity. Collaborate with product development teams to ensure new products comply with all applicable regulations. Conduct risk assessments to identify potential compliance issues and propose solutions to mitigate them. Draft risk analysis reports and present findings. Maintain organized and up-to-date compliance documentation, including certificates, audit reports, and communications with clients/customs/authorities. Assist in the preparation and management of internal and external audits. Support in the preparation of training materials to raise employee awareness of regulations and compliance practices. Participate in internal training sessions to deepen understanding of industry regulations. Work closely with legal, engineering, marketing, and sales departments to ensure all business processes comply with regulations. Facilitate communication between different teams to resolve compliance issues and ensure regulatory adherence. Contribute innovative ideas to improve compliance and regulatory processes. Participate in special projects related to compliance and the implementation of new regulations. Prepare periodic reports on regulatory compliance and activities carried out by the Regulation and Compliance team. Analyze collected data and present results. Assist the Regulation and Compliance team in daily activities such as managing requests, meetings, and preparing presentations. PORTRAIT OF A PERFECT CANDIDATE
You know you are a good fit with the role if:
You do not see problems, you just see solutions. You love challenges and you take your responsibility seriously. You are a real team player. You are an excellent performer with a proven excellence in academic and professional life. You have a bachelor's degree in Electronic engineering. You have a great knowledge of Office package (Excel, Power Point, etc.). Basic understanding of the technologies used in smart eyewear. Interest in technological innovation and ability to understand the regulatory implications of new technologies. Precision and ability to spot small errors that could have significant legal or compliance implications. Proactive approach and creativity in finding practical solutions. Ability to effectively communicate with different teams and hierarchical levels. Capability to manage multiple tasks simultaneously and meet deadlines. Ability to quickly adapt to changes and new challenges. Willingness to learn new skills and continuously update knowledge. Familiarity with medical device regulations, electronic and product safety standards, are a plus. Fluent in English, both written and spoken. You have at least 0-1 years of experience. WHAT ELSE DO YOU NEED TO KNOW?
In EssilorLuxottica you have the feeling of being part of a "success story", no matter where you work in the EL world, you can really make an impact.
This position will be located at our Operations HQ at Agordo (BL).
Are you ready for this challenge?
If yes, we are waiting for you.
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.
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