Quality Officer EMEA
Location: BelgiumSIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science market driven on science, we couldn’t stay behind; we drive Recruitment Science. Investing a majority of our turnover in technology enables us to use unique Resource Technologies. By using highly advanced algorithms, we enable our team of Resource & Data Strategists© to maintain the most advanced, detailed and complete Life Sciences network in Europe. This big data enables us to work Reverse Recruitment©: we first analyze the market in-depth before we go out to the market. Because we analyze the whole market, we can compare facts and data. This enables us to do Facts & Big Data Recruitment©, making sure we, or better yet, you find the right career!
THE COMPANY
Our client is a professional Medical Devices organization, based in Brabant Flamand Belgium.
The company is a big healthcare multinational who produces and sells both drugs, diagnostics and medical devices worldwide. For more than 120 years, they have been successfully developing solutions to the world’s complicated health issues.
ROLE DESCRIPTION
As a quality officer you will be the person ensuring that all the devices produced by the company are compliant to the applicable regulations and standards within the EMEA. You will support the Quality Manager in implementing and maintaining the quality system.
RESPONSIBILITIES
• You will oversee the activities of the company’s country offices of Europe, the middle east and the African continent and its implementation of the quality system
• You will perform internal audits and prepare the quality assurance activities for external audits
• You will provide training in the introduction to quality assurance and SOP to new employees
• Leading QMS continuous improving projects will be your responsibility
• You will support QC processes within your area including CAPA, Change Control, Risk Management, etc.
• Follow-up and monitor the calibration of the medical devices
REQUIREMENTS
• You hold a university degree in science, or have the equivalent working experience
• Background in quality systems and internal audits
• You have an extensive knowledge of MDD, AIMDD and ISO13485 standards
• You are fully proficient in English
• MS Office knowledge
• Be available to travel 25% of your time
• You have no problem with working in teams
• Good communication skills
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Nicolas Gyselinck.
