Specialist in Quality Systems
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 Netherlands.
They are an international market leader in medical technology. Their main focus is on providing healthcare services and solutions to improve our lives. They have a broad range of knowledge and expertise as they are constantly in touch with society. They anticipate immediately on changes and developments within healthcare across the world and therefore, reached more than 50 million people.
ROLE DESCRIPTION
You will become part of a dynamic and technology- driven business setting. As a specialist, you are working with other specialists that focus on quality and compliance of medical devices. Together, your aim is to improve quality systems in which you are supported by designers, manufacturers, and translators. You will receive guidance of the Quality Assurance manager who directs the corporate QA team. This project lasts for 4 months, with a possibility for extension.
RESPONSIBILITIES
As a quality system specialist, you are responsible for the Quality Management Systems in general. You have to make sure that this system corresponds to the vision of both the Research and Technology department and the Translations department. Furthermore, your role includes:
• To be aware of the internal and external regulations including ISO qualifications.
• To prepare processes such as Audits, CAPA, Document control, risk- and supplier management.
• Constantly analyzing the data and processes to identify improvements.
• Taking the lead in applying these improvements within the quality systems.
• To support the management by assessing the latest implementations.
REQUIREMENTS
• Bachelor of Science.
• Minimal 5 years of experience with Quality Assurance and Regulatory Affairs in the Medical Devices industry.
• Minimal 2 years of experience with Quality management systems and ISO qualifications.
• Evidence of problem- solving skills and critical assessment.
• Fluent in both English and Dutch.
• Not to be afraid of taking responsibility and initiatives.
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.
