QA specialist
Location: NetherlandsSIRE Life Sciences® is the market leader in life science recruitment. We believe the recruitment market needs to gear up in technology and continues innovation. We like technology, in a life science 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!
THE COMPANY
Our client is a professional Biotechnology and Pharmaceutical organization, based in Overijssel Netherlands.
They are a worldwide company in the biotechnological field. They focus on ensuring the safety and quality of medicines, vaccines and health care products.
ROLE DESCRIPTION
It is your passion to ensure the safety and quality of their health care products? Do you want to be a part of an important team that contributes on the continuous improvement of those health care products? Are you willing to do an extra step to make sure everything gets done on time? Then this is the job for you! This job will last for 6 months with the possibility to extend.
RESPONSIBILITIES
You will be responsible for Reviewing documents and releasing products. You will be involved during the audits and ensuring the guidelines are followed. Next to that you will be responsible for the following:
- Implementing new processes to improve and ensure this quality
- Maintaining contact with colleagues from production and participate in the daily operational consultation
- Contribute to the existing projects within multidisciplinary teams
REQUIREMENTS
- BSc or MSc within the biotechnology or pharmaceutical industry
- You have experience with recalls and reviewing
- Experience in the pharmaceutical industry and in particular knowledge of GMP
- Knowledge of the relevant computer systems such as Trackwise and SAP
- You have experience with GMP
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Valentijn de Krom.
