Experienced QA specialist

Bedrijfsnaam: -
Plaatsingsdatum: 26/02/2019
Standplaats: -

Functieomschrijving

SIRE® is the market leader in Life Sciences recruitment. We believe the recruitment market needs to gear up in technology and continuous innovation. We like technology, in a Life Sciences 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!Our client is a professional Medical Devices organisation, based in Gelderland Netherlands.The CompanyThis organisation focuses on creating highly innovative and technology-driven products. They are responsible for the development and production of technical medical systems that are intended for the cleaning and disinfection of endoscopes. They have great ambitions and are therefore looking to expand their organisation.

Role DescriptionYou will become part of an informal and dynamic business setting in which quality is set at a high standard. You will receive various responsibilities that are directed to maintain and improve the Quality Management System. In addition, you are responsible for the ISO 13485 standards and required documentation. You will be the key person to contact whenever there are any issues or questions about the Quality system, ISO standards and required documentation. Furthermore, you will gain insights into improvements and developments for the QA department.

ResponsibilitiesOn a daily basis you are involved with overviewing and maintenance of the Quality Management System. In addition, on a daily basis you are involved with:
• Development of strategic plans and implementation tools for the improvement of the Quality Management System
• Gain insight into possible points of improvements for the QMS according to ISO 13485 standards
• Providing advice and support to management in set up of QA/RA processes
• Collecting and creating reports of outcomes from audits especially for CAPA’s
• Management and control of QMS documentation and reviewing these documents
• You will be on track with the latest developments and changes of QA within the Medical Devices sector, involving regulations & legislation such as the MDR and FDA

Requirements• Bachelor or Master 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
• Proven experience with the maintenance and improvement of QMS
• Excellent knowledge of American and European legislation and regulations
• Fluency in English, and good understanding of the Dutch language
• Critical scope and excellent analytical skills
• Team player, yet individual operator


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.

 

Aanbod/arbeidsvoorwaarden
-

Samenvatting

Plaatsingsdatum :
26/02/2019
Referentienummer :
97557
Standplaats :
-
Adres :
-
Postcode :
9723 HK
Opleidingsniveau :
HBO
Uren :
Nader te bepalen
Dienstverband :
Vast
Werkervaring :
3 - 5 jaar
Contactgegevens :
bekijk