Italy Rx Quality Compliance Manager - Sedico, Italia - Operations OO

Operations OO

Azienda verificata

Sedico, Italia

5 giorni fa

Inviato da:

Piero Bianchi

Reclutatore di talenti per beBee

Descrizione

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 cuttingedge 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 motivated, curious and enterprising talent to join us within the RX (opthalmic lenses) business area.

As Italy RX Quality Compliance Coordinator you will work actively helping to coordinate the business activities and strategies related to Quality Compliance.

Below some of the activities you will oversee:

Responsible of quality management system and compliance RX Italy
Management of maintenance and implementation of QMS (ISO 9001, ISO 13485)
Management of documentation of product provided to customer according to medical device regulation (MDR)
Management of relation with notified bodies to organize the certification/surveillance audits

The role allows a 50% of smart work.

The workplace will be Sedico RX plant (Belluno, Italy), with 1 day of travel to a RX Lab in Padova (Italy) when needed.

PORTRAIT OF A PERFECT CANDIDATE

Effective knowledge of MDR medical device regulation (2017/745) and quality system management (ISO13485)
Ability to create a strategy to guarantee the compliance to regulatory requirements and internal policies guidelines
Ability to design documentation and procedures according to regulatory and EssilorLuxottica quality policies
Ability to build a relationship with stakeholders and effective communication skills
Ability to manage and support the business vision on a large scale, oriented and/or experienced in multicultural and multilanguages environments
Curious on market trends and conditions
Time management skills
Able to positively influence others
Analytical and problemsolving abilities

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 EssilorLuxottica world, you can really make an impact.

Are you ready for this challenge?

If yes, we are waiting for you.