QA Engineer Logistics

Location: Netherlands

SIRE 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 leader in Hospital equipment and solutions, cleanrooms and sterilisation departments. They provide an exciting environment with many international opportunities as well as an environment where you can develop yourself. Now they are looking for a junior/starter in QA to support their logistics site.

ROLE DESCRIPTION

As the Quality Engineer you will work on their logistics site near Eindhoven. Here you will join the logistics team and fulfil a key role from their international structured organisation. As a starter in Quality you will be able to develop yourself further and with experience start gaining responsibilities. together with the QA Manager you will be responsible for all Quality projects in cooperation with the plants, offices and sites across the world.

RESPONSIBILITIES

The QA Engineer Logistics is responsible for establishing and maintaining the global logistics Quality Management System and identifying the opportunities for improvement
• Implementing, maintaining and controlling a global Quality Management System based on ISO 13485 and FDA regulations
• Ensure that inbound inspection is maintained with all related processes.
• Coordinating the investigation of the Logistics Complaints in TrackWise and following up on the corrective actions
• Identifying training needs and recommendations to achieve or maintain necessary employee competencies
• Ensure that inbound inspection is established, implemented and maintained with all related processes
• Monitoring performance by gathering relevant data and producing statistical reports
• Ensuring activities in the quality plans are carried out
• Support on logistics related CAPA’s
• Logistics CAPA coordinator
• Participating in internal audits and follow up on the audit findings
• Responsible for monitoring and maintaining quality and compliance targets
• Preparing and analyzing information for the purpose of Management Review

REQUIREMENTS

• Bachelor’s degree in Quality Assurance or related field
• Minimum 2 years hands-on experience in Quality Assurance
• Willing to travel (both nationally and internationally)
• MS Office, Enterprise Resources Systems (ERP)
• Knowledge of ISO 13485 / ISO9001 / FDA and EUR regulatory compliance for medical devices
• Excellent Communication skills

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.