Widen Your Horizons. Join the Next Chapter of Your Career
At EssilorLuxottica, we are committed to empowering our people to grow and succeed. This is your opportunity to take your career to the next level, embrace new challenges, and continue making a difference.
We work for a brighter future, thinking today about the world of tomorrow.
Don't miss the chance to shape your #FutureInSight with us!
GENERAL FUNCTION
The QMS Engineer is responsible for supporting the implementation, continuous improvement, and internal auditing of the Quality Management Systems which govern the processes of medical device manufacturing in our laboratory. The QMS Engineer will also assist in the training of management and associates in QMS best practices for ISO 13485. Manage the internal audit program and report findings to the Quality Manager.
The primary focus of this position is to monitor, maintain, and update the QMS system and ensure compliance to ISO 13485 / 21 CFR 820 FDA and EssilorLuxottica Quality policies and procedures. Duties in this position are usually very repetitive, requiring reviewing process and procedure documents and updating them as applicable. The position will require the ability to work independently as well as across multiple departments.
MAJOR DUTIES AND RESPONSIBILITIES
BASIC QUALIFICATIONS
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.
Associate Engineer • Dallas, TX, United States