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-Holland Netherlands. They are a world leader in healthcare. A company that delivers their part in a healthier world. It is a highly trusted organization with a diverse portfolio in for instance in pharmaceuticals and devices. They have modern production facilities.
Role descriptionYou will be responsible to guard over de quality of our clients products. You will report abnormalities within the production and do quality reviews. Continually you are a part of improving the quality of the products. You will work in a team of QP’s and QA specialists and you are responsible to report to the QP. The end date of this project is not yet known, expected 6-8 months.
ResponsibilitiesAs an interim QA specialist you are responsible for the routine work of Quality Systems activities. Monitor, review and give advice to your colleagues about procedures and standards of Quality Assurance is a part of your function.
- helicopter view in guarding guidelines within QA
- Give training and advise in Quality Systems
- Review product quality and documents of product release
- Implement new processes
- Maintain communication with different departments
- Be part of improvement projects
- Support in QS-subjects as change control, auditing, regulatory compliance etc.
Requirements- BSc. or MSc. in Life Sciences
- 3-5 years QA experience within the pharmaceutical industry
- Experience with GMP and ISO standards and regulatory guidelines
- Fluent in English and Dutch