Quality Assurance Manager
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 Noord-Brabant Netherlands.
They are an international company operating in many different areas such as Patient care, clinical systems, healthcare and imaging systems. They work on projects ranging from treatment, therapy, diagnosis and disease management.
ROLE DESCRIPTION
As the new quality manager you would be focusing with your team on connected health devices and pain relieve. Your work would ensure the quality and safety of products both medical and non-medical in a creative and innovative environment. You will report to the Quality Assurance Lead manager while working and being in contact with divisions such as marketing, procurement and service teams.
RESPONSIBILITIES
Your main responsibilities will be to ensure safety and quality while instructing, coaching, and facilitating project teams regarding regulations and standards.
• Responsible for quality and regulatory compliancy with the QMS and BMS requirements
• Review requirements and manage outcome of all processes
• Review verification and validation
• Make sure that quality of UFMEA, DFMEA, PFMEA etc. is ensured
REQUIREMENTS
• Bachelor degree with 5+ years or master with 3+ years experience of relevant experience
• Applied knowledge of regulations and requirements regarding medical devices such as CFR parts 803 and ISO 13485 and ISO 9001
• Experience in medical device industry
• Creative but detailed while maintaining sight of the goals and the bigger picture
• Fluent in English
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.