Job description
A QA Officer (or QA Manager GMP) is involved in GxP areas – Good Clinical Practice (GCP), Good Distribution Practice (GDP) or Good Manufacturing Practice (GMP) in the manufacturing of pharma products. You have a vital role within Quality Assurance in pharmaceutical manufacturing. Working in the GMP area there is close collaboration with the supply chain to ensure the required quality standards are being met in the supplies and products. In all three areas, the QA Officer ensures that the relevant quality systems are updated with all required information and actions on a timely basis.
Looking for a job as QA Officer?

Your role as a Quality Assurance Officer involves a number of tasks such as batch review, approval of incoming raw material requests and subsequent release, change control and validation-related activities.
In detail, some of the Quality Assurance Officer responsibilities may include the following:
To become a QA Officer you will need a BSc or MSc in biopharmaceutical or biomedical science, chemistry, pharmacy or another relevant Life Science degree. As well as this, a number of years working in the pharmaceutical or food industry is preferred, and up-to-date knowledge of GMP regulations is an advantage.
Personal skills and attributes that you need to bring to the role include:
The salary of a QA Officer depends on experience and the nature of the role being offered. In the Netherlands, it varies between €31.000,- and €60.000,- per annum for full-time positions. Have a look at our QA Officer vacancies to see what’s being offered currently. And talk to us! We may have opportuntities that are not advertised, due to client confidentiality.
See all Quality Assurance Officer vacancies
Is the vacancy you are looking for not listed? Contact us and we will be happy to help you with your dream opportunity! You can also register with Talentmark using the form below.