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

They help their customers accelerate life sciences research, solve complex analytical challenges, improve patient diagnostics, deliver medicines to market and increase laboratory productivity.

Role Description

You maintain the QMS (ISO 9001, GMP), conduct batch releases and support the improvement of processes and manufacturing.

Responsibilities

- Maintain the quality management system
- Keep processes and procedures up-to-date (audits, updating, Thermo Fisher integration)
- Participate in the Management review
- Oversee Documentation control (Local, Consense, Agile, Website, OEM, E1).
- Register/measure non-conformities & improvements, coordinates /implements where necessary.
- Batch release

Requirements

- HBO (BSc) education level
- Knowledge of relevant guidelines in the field of ISO 9001, USDA and GMP/GLP
- Knowledge of Microsoft Office, Trackwise, Agile, ERP

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