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.Job Scope - This person will be responsible for product and manufacturing quality assurance within the Madrid lab working on site Monday to Friday. They will also support the In Market Quality Manager on product quality items affecting his Area.Areas of responsibilities and related activities :Lead and manage the Manufacturing Quality team.Follow up of the existing KPI's of quality assurance and definition of new ones.Define and implement corrective and improvement plans for manufacturing processes.Support when required in the analysis of clients' technical returns.Coordination with the engineering and operations department for projects related with processes improvements.Supervision of the implementation of action plans derived from surveys and audits.Deploy the necessary instructions for compliance with the regulations of CE marking, ISO 13485, ISO 9001 and ISO 14001 of Medical Devices, Quality and Environment and Prevention of Occupational Risks in accordance with the systems implemented in the company.Responsible for the surveillance system to comply with R.D. 1591/2009, of October 16, which regulates medical devices. It will be an interlocutor and collaborate with the Health Authorities in relation to incidents of manufactured and imported products.Network of Interaction :Internal : Production, Engineering, Customer ServiceExternal : Customers, Quality MEA, Global EngineeringPreferred requirements/competencies :Industrial Profile - At least 2 years of experience in QA in multinational companies within the manufacturing sector. Experience in team management will be valued. ISO 9001- ISO 13485. QMS. Valuable lean methodology knowledge. Fluent English and Spanish .#J-18808-Ljbffr