QUALITY & COMPLIANCE MEDICAL DEVICE INTERN

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 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 support the quality team in different areas.
Here some responsibilities you will have.
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.
PORTRAIT OF A PERFECT CANDIDATE   Each and every one of us lives, breathes and shapes the success of the company.
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 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     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 , in accordance with Article 15 of Stat.
Lav and Legislative Decrees and .