Quality assurance 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 Pharmaceutical organization, based in Overijssel Netherlands.
They are a committed company to help you live your best possible life through the power of health. They push the boundaries to help manage and treat health challenges. People at this company come to work each day with relentless energy, enthusiasm and a promise to enhance the health and well-being of millions of people.
ROLE DESCRIPTION
Do you want to be actively involved as quality assurance specialist in the production, including when there have been deviations during the production process. Also monitoring, reviewing and advising colleagues on procedures and standards that the company has. You will need to keep an overview and monitor the guidelines surrounding the quality of our products. Next to that producing product quality reviews and implementing new processes to improve and ensure this quality are part of your tasks.
RESPONSIBILITIES
You will maintain contact with colleagues from production and participate in the daily operational consultation. Next to that you will review documents and release products. Other responsibilities will include:
- contributing to improvement projects within multidisciplinary teams
- The investigation and responding on product complaints
- Supporting government and customer audits
- Supporting the QPs within the department
REQUIREMENTS
- BSc or MSc within the biotechnology or pharmaceutical industry
- Experience in the pharmaceutical industry and in particular knowledge of GMP
- Knowledge of the relevant computer systems Trackwise, Solid, SAP
- You are someone who dares to go to clients and employees and show conviction
- You need to have an energetic working attitude and like to work with people from various departments and different courses
- Dutch and English are required
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.
