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 and Biotechnology organisation, based in Noord-Brabant Netherlands.

The Company

Our client is a Pharmaceutical Start-Up that is growing (very) rapidly.

Role Description

You are responsible for a broad variety of quality tasks.

Responsibilities

- Release of product
- Improvement of the QMS
- CAPAs, Changes, Deviations
- Validation & Qualification
- Auditing (internal/external)
- Contact with authorities, colleagues, CMO's, CRO's

Requirements

- A life science degree or related (or relevant work experience)
- Experience in a GMP environment (Pharmaceutical or BioTech company)
- Good language skills in English (Dutch is a plus).

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