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 Biotechnology organisation, based in Zuid-Holland Netherlands.

The Company

Biopharmaceutical client who is dedicated to bring therapies that will significantly improve patients lives.

Role Description

You are responsible for monitoring and improving the quality of the production and Quality System. You are a quality expert who works closely with all supply chain departments.

Responsibilities

- You are part of the deviation team:
- Apply QMS per GMP standards
- Handling deviations, monitor quality of Root Cause investigations
- Review investigation reports
- CAPA’s, change controls
- Participate in quality projects and projects for New Product Introduction

Requirements

- BSC./ Bachelor Biochemistry, Biology or a pharmaceutical degree
- 5 to 7 years relevant working experience in a GMP environment
- Fluent in English, Dutch is a pré
- Available within 1,5 month