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

They are an international organization who focus especially on services in pharmaceutical development of products that are focused on curing different diseases. A company that belong to the top in pharmaceutical in the world.

Role Description

Currently we are looking for a QA consultant. You will work in the QA department. The end date of this project is not yet known, expected 6-8 months.

Responsibilities

You will be responsible for complaint handling in the area of SME related processes and GMP. You will log, report and complete the complaints in due time. To contact the stakeholders is your responsibilities. The investigations need a follow up.
- Work together with quality specialists
- Work with GMP system
- Knowledge of pharmaceutical product development, testing and releasing
- knowledge of qualification, manufacturing, validation

Requirements

- BSc. MSc. in a related area such as Pharmacology
- 1-3 years of experience in related area
- Experience with pharmaceutical GMP systems
- Fluent in English and Dutch with excellent communication skills