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 Pharmaceutical organisation, based in Antwerpen Belgium.

The Company

Onze klant is een Farmaceutisch / Medical Device bedrijf in de regio Sint Niklaas tussen Antwerpen en Gent.

Role Description

In deze rol bent u verantwoordelijk voor kwaliteit in een GMP en/of ISO13485 omgeving.

Responsibilities

- Quality Specialist Root-Cause
- Aanspreekpunt voor klantenklachten
- Root Cause Analyse klanten- en interne klachten
- Analyse klachten (leveranciers-, klanten-, interne klachten)
- CAPA’s n.a.v klachten

Requirements

- Ervaring met klachtenbehandeling
- Ervaring in GMP of ISO13485
- Nederlands sprekend

Heb je interesse en wil je meer weten over deze functie, reageer dan door op solliciteer te klikken en contact op te nemen met Daniel Woudenberg