QA Engineer Manufacturing

Bedrijfsnaam: -
Plaatsingsdatum: 25/10/2018
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 Brussels Hoofdstedelijk Gewest Belgium.The CompanyThis organisation is developing high-technology products across the globe. They focus on the improvement of our health within society. As a continuously growing company they are looking for new specialists.

Role DescriptionIn your role as Quality Engineer, you will be operating at the manufacturing site. On a daily basis you will have to establish and maintain relationships with various stakeholders within the organisation. You will overview all activities attached to Quality Assurance of the site. Your major task is to advice the engineers and support the team in relation the QMS. Furthermore, you will be assisting that department in collecting required documentation and regulations. You will directly report to the Quality manager.

ResponsibilitiesYour main task is to be on the site as QA expert that supports and advises various stakeholders which are directly involved in manufacturing. Furthermore, your role includes:
• Maintain and establish relationships with internal and external stakeholders in the USA and Japan
• Improve and maintain the QMS according to ISO 13485 and ISO 9001 standards
• Providing 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 engineering
• Minimal 4 years of experience within the Medical Devices
• Excellent knowledge of quality standards such as ISO 13485, 21CFR820, GMP
• Excellent knowledge of EU and USA regulation for Medical Devices
• Experience with root cause analyses, CAPA’s, and Risk management
• A team player, yet strong individual
• Fluency in English and Dutch, preferably Business level French
• Strong communicator and 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.

 

Aanbod/arbeidsvoorwaarden
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Samenvatting

Plaatsingsdatum :
25/10/2018
Referentienummer :
95967
Standplaats :
-
Adres :
-
Postcode :
9723 HK
Opleidingsniveau :
HBO
Uren :
Nader te bepalen
Dienstverband :
Vast
Werkervaring :
3 - 5 jaar
Contactgegevens :
bekijk