Quality Assurance Engineer
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 organisation producing Medical solutions and devices. They have multiple offices and operates in more than 40 countries and have sales in more than 150. They offer and stimulate a growth for their employees and are looking for a (junior) QA engineer to support the logistics office.
ROLE DESCRIPTION
As the new Quality Assurance Engineer you will implement, maintain and control a Global Quality Management System that is based on ISO 13485 and the regulations of the FDA. You will work with the local QA Manager and be supervised by the Benelux QA Manager to identify opportunities to grow and stimulate improvement.
RESPONSIBILITIES
Besides being responsible for the QMS you will be responsible for:
• Coordinating the Post Market Surveillance and complaint management and following this up with Corrective and Preventive Actions.
• Ensuring that inbound inspections are established, implemented and maintained with all processes at the logistic site you will work
• Performance monitoring by gathering relevant data and as a result producing statistical report for assessment
• Participating in internal audits
• Responsible for maintaining and monitoring quality and compliance targets conform the company strategy.
REQUIREMENTS
• Knowledge of ISO 13485, and ISO 9001 (FDA is a big plus)
• Willingness to travel both nationally and internationally
• Fluent in English is a must, Dutch is an added value
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.
