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, Chemicals and Biotechnology organisation, based in Limburg Netherlands.
Our client encourage their employees to challenge themselves. Or client strives to be the leading supplier to improve the quality of life by using science and technology.
They work with passion to transform life science into new possibilities for their customers.
Do you want grow in your career and help our client to do better?
Our client have a multi national and multi lingual team, where you will be working at as Senior Quality Assurance Officer.
You will be responsible for planning and execution of daily quality assurance activities. At the same time you have to ensure compliance with international quality requirements.
You will do that as defined by the applicable guidelines (e.g. FDA, EMA, ICH). It is also important to do this by the existing GMP standards in the area of responsibility.
A good company with great opportunities! As Senior Quality Assurance Officer you will do the following tasks :
You have to plan and execute quality assurance activities, think of document management, batch record and label issuance, batch record review, equipment and supplier qualifications, including documentation.
You also will monitor compliance. Think about GMP and safety standards in the area of quality assurance.
You will support the Qualified Person in his role with audits and quality training. Your other responsibilities are :
The requirements you need to have for this role, are :
Are you accurate, self-organized, flexible, a real team player and do you have attention to detail? Than you are the one they are looking for!
Don't wait, don't doubt, and just apply!
Are you interested and do want to apply for this role, please fill out your application via the apply button below and contact Diana Prieto Reyes.