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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 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.
Onze klant, een toonaangevend biofarmaceutisch bedrijf, is op zoek naar een QA Specialist voor een multiproduct Drug Substance productiefaciliteit. De focus van deze functie ligt op het waarborgen van de hoogste kwaliteits- en compliancenormen door middel van actieve quality oversight op operationele processen en documentatie.
Our client, a leading pharmaceutical organization, is seeking a senior expert to support their production and supply chain facility. This role focuses on providing quality oversight and acting as a subject matter expert for cleaning validation activities to ensure regulatory compliance and reliable supply.
Our client, a prominent pharmaceutical organization, is seeking a Quality Specialist Operations to focus on quality oversight and project support. The role involves managing operational quality tasks and ensuring compliance within a strictly regulated production environment.
Our client, a technical solutions provider for the life sciences industry, is seeking a Technical Writer to manage critical documentation and validation processes. This role ensures the high-quality delivery of technical manuals and validation protocols for both internal production and external client sites.
Our client, a leading pharmaceutical company, is seeking a CSV Engineer to support the validation of cGMP-critical computerized systems. The role focuses on ensuring systems remain compliant with applicable regulatory and quality requirements through hands-on validation activities.
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.
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