18.11.2018 18:03

Compliance specialist (zagranica)

SIRE Life Sciences® - Opublikowano: 18 lis 2018
SIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences 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!Our client is a professional Medical Devices organisation, based in Antwerpen Belgium.The CompanyThis international organisation is specialised in women and child healthcare. Their focus is on the innovation and development of hygiene products. They highly prioritize sustainability and quality. As they are expanding, they are looking for a Quality Expert.Role DescriptionAs a quality expert, you will become responsible for the Quality Management System. You are key when it comes to the maintenance and improvement of the QMS. You will collaborate closely with different sites of the Holding. You will receive the responsibility to connect various activities for quality, environment, and safety. Furthermore, you are reviewing the regulatory aspects and you will collect required documentation. Finally, you will be the contact person when it comes to the establishment and maintenance of internal and external stakeholders.ResponsibilitiesAs mentioned previously you are mainly involved with the Quality Management System. In addition you will be involved with:• Maintenance and achievement of certifications such as the ISO 13485, ISO 9001 and the ISO 14001• Guidance during the execution of audits from the beginning to the end• Support of Group Holding to achieve international and European labels for the environment, safety and quality• Monitoring and researching trends and developments in relation to these standards• Improve, expand and overview required documentation, policies and proceduresRequirements• Master Degree in Engineering• Minimal 3 years of experience with the Medical devices industry with significant experience regarding certifications• Minimal 2 years of experience in a Quality management position• Proven experience with the maintenance and improvement of QMS • Fluency in English, and good understanding of the Dutch language• Critical scope and excellent analytical skills• Ability to maintain and establish relationships• Team player, yet individual operatorAre you interested and do want to apply for this role, please fill out your application via the apply button below and contact Juliette van Kraaij....