Quality Engineer to Cochlear in Gothenburg

Cochlear Bone Anchored Solutions AB is a medical device company and the world leader within bone anchored hearing solutions.Its head office is based in Mölnlycke, outside Gothenburg.Cochlear Bone Anchored Solutions AB is part of the Cochlear group which is the world leader within hearing implants.The turnover for the total Cochlear group is 3.6 Billion SEK and the organization employs over 1800 people worldwide.Visit www.cochlear.com to learn more about Cochlear and how our products Baha and Vistafix improve the quality of life for people all over the world. Quality Engineer to Quality and Regulatory Department at Cochlear Purpose of role To continually improve and develop the quality system in order to secure that it is always in compliance with applicable standards and current practice. Key responsibilities - Responsible for the planning and implementation of Internal Audits.- Participate in 3'rd party Audits and be responsible for corrective actions when necessary.- Responsible for the company's system for Corrective and Preventive Action.- Active participation in the drafting and implementation of Quality Procedures.- Provide advice and training on Quality System Requirements.Act as a Project Manager for various Quality System related Projects.- Review CAPA's and initiate improvements when necessary.- Review non-conformities in Manufacturing and initiate improvements when necessary.- Assist all internal departments with development of Internal Procedures and Processes. Key requirements - Experience of planning and implementing Internal Audits - Experience of quality work from Production/Manufacturing Environment - Experience of Project Management related to Quality Process Improvements/Change Management Concern for Order & Quality - Relationship building: Cooperate with all departments and give necessary support.- Training capabilities: Ability to communicate and train the organization in BAS Quality System - Excellent English language skills - Academic degree: Engineering or similar Experience from Regulations and Quality Systems for Medical Devices (MDD, ISO 13485 / FDA QSR) is considered an asset. Personal profile Organized and motivated by results.Able to work within stressful environments, yet remain calm and able to deliver.Team player who can work within the development team values: Courage, collaboration, excellence, freedom with accountability and respect.Customer service orientation: Acts to makes things better for customers. What can Cochlear offer you?Great team environment.Opportunities for ongoing learning and career development.International and inspiring company culture Application and contact This recruitment is managed by Flexlife AB.If you find the role challenging and interesting, please apply through www.flexlife.se.Submit your application as soon as possible.Interviews will be held continuously.