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 Netherlands.

The Company

Our client is an international pharmaceutical company located in Breda. Focused on biotechnology and biochemistry research, their product portfolio encompasses the areas of oncology, kidney diseases, bone diseases, hematology and cardiovascular diseases.

Role Description

In this role you will responsible for all the Quality Assurance activities related to a production line, and support the final product release.

Responsibilities

- Perform batch reviews records and support production areas.
- Act as first point of contact for production staff during packaging and labeling operations.
- Perform finished product checks before commercialization.
- Support compliance with SOPs and ensure GMP.

Requirements

- At least MBO or Bachelor's degree in Life Sciences field
- 2 years of experience in a QA position or manufacturing experience (pharmaceutical or medical device)
- Knowledge of GxP is highly advantageous
- Availability to work in (3) shifts

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