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 Flevoland Netherlands.

The Company

A biotech company in Lelystad providing the highest quality for the clinical trials of their customers.

Role Description

In this role you are responsible and have a central role in building up and implementing the quality management within the company.

Responsibilities

Together with the rest of the company you serve your customers with finding solutions for their research challenge and for that raising your quality system from ISO 9001:2015 to GMP, providing the highest quality for the clinical trials of your customers.

Requirements

The ideal candidate has at least five years of experience in a GMP environment and is familiar with internal and external audits.
MSc. in relevant field
Knowledge of quality management systems
Excellent communication skills in English

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