Ad Interim Quality System specialist

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 Friesland Netherlands.

This client is an expert in technological development within the Medical Device sector that focuses on the improvement of diagnostics and medical discovery. They set up clinical laboratories and enable medical research for particular diseases, cancer, surgical procedures and infections.

ROLE DESCRIPTION

Quality is set at a high standard. You will focus on the Quality Management System and required documentation for the European and US standards. On a daily basis you are supporting the QA team in the development and improvement of the Quality System. You will be creating procedures and strategies that ensure that the devices are compliant with both internal and external regulations and quality standards. You will be the contact person when it comes down to issues regarding Quality Assurance and particular standards. This project is for a period of 8 months with a possible extension to 10 months.

RESPONSIBILITIES

As Quality specialist your main responsibility is to increase and maintain the Quality Management System and involved documentation. Furthermore, you are involved with:
• Collecting and creating reports of outcomes from audits especially for CAPA’s
• Identifying points of development for the QMS and making adjustments in relevant documentation
• Creating awareness of importance RA and QA within the corporate organisation by using internal resources
• Providing advice and support to management in set up of QA/RA processes
• Management and control of QMS documentation and reviewing these documents
• Execution and guidance during internal and external audits, and being the contact person for any occurring issues
• Assisting in the development of trainings and tools regarding quality issues

REQUIREMENTS

• Bachelor in Life Sciences
• Minimal 4 years of experience with QA on a production site within the Medical devices industry
• Minimal 2 years of experience in an strictly regulated environment
• Excellent knowledge of the ISO 13485 standard
• Experience with the maintenance and improvement of QMS
• Experience with SAP and TrackWise
• Team player with extraordinary communication skills
• Fluency in English, and good understanding of the Dutch language
• Experience as auditor for both internal and external stakeholders
• Critical scope and excellent analytical skills

Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Juliette van Kraaij.