QA Officer
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 Healthcare and Medical Devices organization, based in Brabant Flamand Belgium.
As a global leader in manufacturing high tech products and materials, our client is looking for a new professional to join the quality team. The company has a high international reputation, providing their customers with the best solutions through their use of cutting edge technology. Their products have a very broad spectrum of applications including the healthcare, dental and automotive industy.
ROLE DESCRIPTION
As the QA officer, you will be responsible ensuring the production, processes and management systems are all in line with the latest regulations and standards. The implementation and continuous improvement will be one of your main focuses during the job.
RESPONSIBILITIES
• You will support the project teams by providing them with quality information during the development or improvement of products
• You will also support the teams on compliance with standards such as ISO13485, FDA QSR and the European MDD
• You will perform research and develop applications to further improve the quality processes and risk management system
• You will be responsible for validation and verification activities, test protocols, process controls and reports
• Performing internal quality audits
• You will be the person setting up technical documentation for both national and international regulatory submissions
• You will be the point of contact to address business and quality production issues
REQUIREMENTS
• You hold a bachelor degree, preferably in engineering
• At least three years of experience in a quality and regulatory environment, such as MD, food, pharmaceuticals, etc.
• Good knowledge of ISO13485 and GMP
• You have a proficient level of English
• You’re able to write clear and understandable engineering specifications for the products
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.
