QA & RA Specialist

Bedrijfsnaam: -
Plaatsingsdatum: 04/10/2018
Standplaats: -


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 Brabant Wallon Belgium.The CompanyThis international market leader is specialised in bone and spine devices. They are operating both with Healthcare professionals and clients. They offer a dynamic and international work environment.

Role DescriptionAs a Quality & Regulatory Specialist, you will gain full responsibility of the Quality Management System, related activities and regulations on the local site for the EMEA region. You will take the lead when it comes to Quality and Regulatory activities. On a daily basis you will assess and review the Quality Management System to see if there is need for any changes and/or improvements. You will be a key contact person when it comes down to questions or issues related to Quality for both internal and external stakeholders. Furthermore, you are also responsible for creating awareness and taking initiatives regarding quality within the organisation. Finally, you are responsible for creating awareness for quality and for the development of training.

ResponsibilitiesYour priority will be the maintenance and improvement of the QMS. Further responsibilities involve:
• Maintenance of the internal and external regulations including ISO qualifications.
• To overview processes and applications conducted by your team which includes
supplier reviews CAPA’s , Document control, and risk management
• Taking the lead in the execution of internal and external audits
• Ensuring compliancy for both Quality and Regulatory principles according to
international stakeholders and notified bodies
• Constantly analyzing data and processes to trace risks and identify improvements
for the Quality Management Systems.
• Maintenance of relationships with both internal and external stakeholders

Requirements• Bachelor in Life Sciences
• Minimal 4 years of experience in the Quality Field
• Minimal 2 years of experience with regulations and documentation such as the
• Excellent knowledge of ISO 1348: 2016
• Excellent organizational and problem-solving skills
• Experience with FMEA, CAPA’s, and risk management
• Experience in leadership
• Fluency in English, French and Dutch
• Strong in 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 Juliette van Kraaij.




Plaatsingsdatum :
Referentienummer :
Standplaats :
Adres :
Postcode :
9723 HK
Opleidingsniveau :
Uren :
Nader te bepalen
Dienstverband :
Werkervaring :
3 - 5 jaar
Contactgegevens :