Quality Assurance expert near Utrecht
Location: NetherlandsSIRE 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 Utrecht Netherlands.
This organisation focuses on a set of services within clinical research, studies and trials within the Medical Devices sector. They perform studies all over the world deviating from cardiovascular surgery to interventional radiology. They are experiencing a rapid growth in which they are in need for Quality Assurance experts.
ROLE DESCRIPTION
Quality is set at a high standard within this organisation. As a QA expert you will become part of a dynamic business setting. The most important responsibility within your daily routine is to assess the performance and maintain the Quality Management System. You will have a supportive role in which you evaluate processes and report critical points of improvement, directly to the QA manager. Next to that, you are in charge of the control of all regulatory and quality assurance documentation. This role can be filled in for 4 months with possible extension to 6 months.
RESPONSIBILITIES
• Development practical trainings and records for internal and external stakeholders
• A critical role within the development of quality projects
• Create and assess an overview of their Key Performance Indicators
• Offer guidance in the entire audit process from the beginning to the end
• Maintain and improve the standard operating procedures
• Order all documentation and create a strategic logic organization of documentation and files
REQUIREMENTS
• Master Degree in Life Sciences
• Minimal 6 years of experience with QA in Medical Devices Branch
• Excellent knowledge of ISO 13485, and broad knowledge of ISO 9001
• Fluency in English and Dutch
• Great eye for detail
• Experienced in strategic planning and excellent organizational skills
• Strong communicator both verbally and on paper
• A team player with a hands-on mentality
Are 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.
