SIRE® 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 companyOur client is a professional Pharmaceutical organization, based in Noord-Brabant Netherlands. They a world leader in healthcare. A company that delivers their part in a healthier world. In over 140 counties they help people and animals with medicals, vaccines etcetera in an innovative way. If you like to be challenged in your work, this is the company to work for.
Role descriptionYou will be responsible to ensure cGMP compliance for the quality systems. On the site you will make sure you get insight in the quality and compliance. It is your responsibility to develop, improve and maintain the Quality Systems including the QMS strategy. The end date of this project is not yet known, expected 6-8 months.
ResponsibilitiesAs an interim QA officer you will focus on coordinating and improving the quality policy. You have the ability to optimize the current work methods and take a leading role in this part.
- Lead internal and external audits
- Coordinate Health Authority inspections
- Promoting Lean behaviors and manage your team
- Coordinate, describe, document, research the processes
Requirements- BSc. or MSc.
- At least 5 years of QA experience within the pharmaceutical industry
- Experience within regulated environment
- Project management skills
- Fluent in English and Dutch