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 Noord-Brabant Netherlands.

The Company

It's a leading company in the field of registration, marketing and sales of high-quality generic medicines, biosimilars and branded products.

Role Description

You will focus on the continuous improvement of the quality assurance system and your own GMP / GDP processes as well as the monitoring and control of the pharmaceutical processes of the ASM and suppliers with which you collaborate.

Responsibilities

You are responsible for the development and implementation of the quality policy and you ensure that files, processes and products comply with prevailing quality requirements from legislation (EU GMP, GDP and the Pharmaceutical Regulations) and the corporate procedures of the parent company.

Requirements

- MSc in Pharmacy
- QA / RA experience in the Pharmaceutical industry
- 2+ years experience as a manager
- Result-oriented, social, communicative and a team player
- Fluent in Dutch and English in speech and writing

Heb je interesse en wil je meer weten over deze functie, reageer dan door op solliciteer te klikken en contact op te nemen met Bram Reulen