Medical Device QMS Auditor

We exist to create positive change for people and the planet. Join us and make a difference too. · Do you believe the world deserves excellence?We are BSI (British Standards Institution), the global business standards company that equips businesses with the necessary solutions to ...

We exist to create positive change for people and the planet. · Join us and make a difference too. · We are looking for a Medical Device QMS Auditor who will analyze quality systems and assess ISO 13485, CE Marking and MDSAP schemes. · ...

We're Hiring | Quality Management System (QMS / SGC) Leader We are looking for an experienced Quality Management System Leader to join our automotive team. · Manage and maintain the QMS in accordance with automotive standards. · ...

A Quality Systems Engineer is responsible for implementing and maintaining the organization's Quality Management System (QMS). They must ensure compliance with regulations and customer requirements. · ...

Responsible for the implementation and maintenance of the Quality Management System (QMS) to ensure compliance with regulations and customer requirements. · ...

We're Hiring | Quality Management System (QMS / SGC) Leader. Manage QMS in accordance with automotive standards. · Manage and maintain QMS. · Plan internal audits. · ...

The QMS coordinator supports all aspects of the management systems audit process through audit planning execution reporting follow-up and re-audit. Ensures the ongoing effectiveness and efficiency of the business management system including its compliance to applicable industry s ...

· Yazaki is a global leader in the research development and delivery of vehicle power and data solutions. · We are looking for energetic people with the potential to perform and strengthen - and thrive in - our positive work environment. · ...

h2Job summary/b/h2>The Quality Management System Coordinator supports all aspects of the management systems audit process through audit planning, execution, reporting, follow-up and re-audit. Primary goals are to ensure the ongoing effectiveness and efficiency of the business man ...

The Quality Systems Engineer will support the development, maintenance, and continuous improvement of the company's Quality Management System (QMS). The role requires strong analytical and communication skills as well as collaboration cross-functionally. · ...

The Quality Systems Specialist is responsible for supporting, maintaining and continuously improving the Quality Management System. This role supports quality system processes including document control, · training, · change control nonconformance, · CAPA activities. ...

Leads audits and supervises changes to the Quality Manual under direct supervision. · ...

We hire talented Failure Analysis Engineer for our company. We strive to create value for our customers by working to improve and extend the return on investment in solid state lighting systems. · Perform sample preparation and initial assessment of defective, electronic, electri ...

Practicante en sistemas de gestión de calidad con beca mensual $7, · 000. · ...

Inventronics is looking for a talented Failure Analysis Engineer to perform sample preparation and initial assessment of defective parts. The role involves writing reports, implementing laboratory equipment, and coordinating technicians. · ...

Ensure compliance, maintenance, and continuous improvement of the quality management systems according to applicable international standards (IATF 16949, ISO 14001, ISO 45001, · Conduct internal system audits according to the annual internal audit plan for ISO/IATF 16949. · ...

Our mission is to be the leading digitally enabled assurance provider, helping our clients navigate a changing risk landscape. We will achieve this by being the leading assurance provider in key sectors including cybersecurity, food, and low-carbon energies, aerospace and automot ...

+The Director of Global Quality Systems & Reliability is responsible for implementing and harmonizing quality management systems across the global manufacturing footprint. · +* Lead the deployment of a unified Quality Management System (QMS) across all identified Electrical manuf ...

As a member of our global team you can expect exciting varied responsibilities as well as a wide range of development prospects. · ...

This role ensures full compliance with FDA regulations (QMSR / 21 CFR 820), ISO 13485, · and applicable international regulatory requirements. Bachelor's degree in Engineering, · Quality, Regulatory Affairs, · or related field. · 7+ years of experience in medical device manufactu ...