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 Gelderland Netherlands.
They are a world leading Manufacturer in Medical Devices committed to life enhancing solutions and exceeding patients expectations in Health Care.
ROLE DESCRIPTION
Due to growth and change of management strategies the company is looking for a new Quality Assurance Officer in their Dutch HQ. You will be under the supervision of the Director Quality and Regulatory Affairs and will be responsible for most of quality related affairs in the company. You overall task is to Manage European and Local Quality activities conform all regulations that are applicable.
RESPONSIBILITIES
• Implement and maintain improvements in QMS for new audits and reviews
• Complaint handling, Post Market Surveillance, CAPA’s, SCAR’s
• Updating the Quality Management System and play a support role for other regions in this
• Responsible for quality of the end product including processes, quality holds and waste management
REQUIREMENTS
• A science related background with at least a bachelor degree
• 3 to 5 years of relevant working experience within Medical Device environment
• Deep knowledge and understanding of ISO 13485, MDD, MDR, FDA
• Fluent written and speech in English and Dutch
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.
