)
Keep documentation and processes compliant with regulation. Deviations, change control and batch documentation are your daily work, at the companies that shape modern medicine.
Onze klant, een toonaangevend farmaceutisch bedrijf, is op zoek naar ondersteuning voor batch-gerelateerde documentatie binnen een GMP-omgeving. De focus van het project ligt op data-integriteit van kleine apparatuur en het beheren van kwaliteitsdocumentatie zoals deviaties en CAPA's.
Onze klant is een internationale organisatie gespecialiseerd in de farmaceutische verpakkingssector. In deze rol ben je verantwoordelijk voor het op niveau brengen en houden van de validatiestatus van systemen, processen en installaties conform de geldende farmaceutische wet- en regelgeving.
Our client, a leading pharmaceutical organization, is seeking a QA Officer to provide quality documentation support and operational quality assurance. This role focuses on maintaining high standards through risk assessments and documentation review while staying connected to the shop floor.
Our client, a pharmaceutical organization, is seeking an experienced professional to ensure quality readiness and compliance for the startup of a new production facility. The role coordinates quality-related activities during the facility qualification phase to ensure a seamless transition from construction to operational status. This position maintains full regulatory compliance and GMP standards throughout the commissioning process.
Our client, a leading life sciences organization, is seeking a specialist to provide quality oversight and functional governance for computerized systems. The role combines independent QA-CSV validation support for manufacturing automation with the site-wide implementation of a digital checklist management system.
Our client, a leading pharmaceutical organization, is seeking a QA Qualification Engineer to provide quality oversight for process and laboratory equipment. This role focuses on managing qualification activities throughout the system lifecycle to ensure strict compliance with international regulations and quality standards.
You do your work. We take care of the rest. Clear agreements and real support.
One dedicated Talent Manager who knows you, coaches you and thinks along with your next step. Before, during and after every project.
From an electric company car to 32 days of holiday. We discuss your expectations openly in the first conversation.
Decades of trusted relationships with leading pharmaceutical players give you access to projects you would not reach on your own.
Workshops, masterclasses and training, from Lean Six Sigma to project management, at your own pace.
Life Sciences projects tend to run long, which gives you stability. We plan your next step well before a project ends.
Every document you keep in order and every deviation you close helps a safe product reach a patient.
For most QA roles, yes, usually at master's level. A first work experience is a real plus. We look at the match with the role, not only your diploma.
For most QA roles in Belgium, yes. You work closely with production and other departments, so a good command of Dutch matters.
Often, yes. Many consultants move into QA from lab, validation or production. Consulting makes that switch possible.
Both. QA is a mix of documentation work and time on the production floor with your stakeholders.
We are happy to answer your questions or help you find your next project as a Quality Assurance Officer.
)
