QA Engineer Logistics

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.

Fast growing/changing Medical Devices company.

ROLE DESCRIPTION

The QA Engineer Logistics is responsible for establishing and maintaining the global logistics Quality Management System and identifying the opportunities for improvement.

RESPONSIBILITIES

- 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 at Logistics Locations.
- 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
- 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.