This is a position at a biopharmaceutical company, where you will be working as a specialist concerning Computer System Validation (CSV). It is possible to work remote most of the time, if you prefer. Working at location in Limburg is also a possibility.
In this job as Quality System Specialist, you will join a dynamic QA team within a global biopharmaceutical company in Limburg area (remote working possible). In this job you will be responsible for all quality related aspects when it comes to the use of computerized systems. You ensure compliance of all computerized systems (hardware and software) by making sure all these systems are qualified and validated in line with GMP regulations.
Hereto, you write/review, implement and maintain all QA related documentation for use of computerized systems.
You will act as a subject matter expert regarding computer system validation and set requirements for the configuration, validation, implementation and maintenance of automated quality systems.
Wie zoeken we?
For this position we are looking for a quality professional with the following background:
- BASc or MSc degree in the area of biotech, biomedical or similar
- Several years of work experience within QA and good knowledge of GMP guidelines
- 2+ years of work experience within CSV
- Fluent in English
- Eligible to work in The Netherlands
- Preferably living within 1 hour travel distance of Limburg; to be able to visit the site every now and then
Wat bieden we aan?
Terms & Benefits:
- Temporary position for 6 month with the possibility for extension
- Competetive salary (€5500- €6500 depending on experience)
- Working hours: 32-40 hours/week
- Opportunity to work most of the time remote, if preferred
Over Science@Work
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