Quality Assurance Manager Benelux
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 Brussel Belgium.
They are an international leader in medial solutions and providing lifesaving care with their expertise. They stand for passion and enthusiasm where there is plenty of space for ideas and initiative. They still grow and due to restructuring they are looking for a new Quality Manager that can support the sites in Hilversum in the Netherlands, and Brussels in Belgium.
ROLE DESCRIPTION
Your purpose and main task is to establish and maintain the global Quality Management System and with that identify the opportunities to improve the systems and overall quality processes. Based on ISO 9001 and ISO 13485 you will implement, maintain and control the systems on both sites. Depending on where you live you will work at least 80% on one site and when needed work 20% on the other.
RESPONSIBILITIES
• As the QA Manager and end responsible you will lead investigations of Non-Conformities and follow up with Corrective Actions, as well coordinate Field Safety Corrective Actions (FSCA).
• Assess and identify training needs to maintain necessary employee skills and competencies.
• Participate in Audits in both the Netherlands and Belgium and inbound inspections.
• Ensuring that activities in the quality plan are carried out according to the quality/company targets and strategy.
• Monitoring performance and prepare and analyze date for statistical reports and management reviews.
REQUIREMENTS
• A minimum of 2 years hands-on experience in QA
• Willingness to travel between Brussel and Hilversum
• Working knowledge of ISO 9001 & ISO 13485, EU regulatory compliance for Medical Devices
• Fluent in French, English and Dutch
• Excellent 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 Jeroen Evertsen.
