Quality Assurance Officer
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 Limburg Netherlands.
The company is a global leader in the development of lab and surgery medical devices. They stand for quality and safety of their products in meeting the patient expectations and ensuring their safety and health.
ROLE DESCRIPTION
They are looking for someone to join the team that is currently expanding rapidly where you will take on the task to set up the new quality team that will join the current forces of the company. With this team you will ensure that all products and processes meet company and regulatory standards concerning the quality.
RESPONSIBILITIES
As the new officer you will report to the Manager Quality Assurance and Regulatory Affairs and supervise your own team and the work done according to the strategy of the company. Your responsibilities will consists of:
• Plan, asses and control all quality testing concerning in process inspections and final products
• Review all test results and analyses where improvements need to be done to meet regulatory and quality standards
• Leading assessment plans arisen from non-conformities and report results
• Participate in new hiring processes for the new team and train team-members
REQUIREMENTS
• A technical/science degree or similar
• 3+ years within Quality Assurance and Medical Devices ISO 13485
• Quality control/Assurance experience within a production environment
• Knowledge and working experience within a highly regulated environment and quality systems
• Experience with ISO 9001 is preferable as well
• Able to communicate and lead on different levels of the company
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.
