Our client, a leading pharmaceutical organization, is seeking an experienced professional to oversee quality and validation activities at their facility. This role ensures that all commissioning, qualification, and validation processes meet rigorous quality standards and regulatory requirements throughout the project lifecycle.
Validation Engineer
Description
The Validation Engineer is responsible for the development, implementation and execution of validation activities for cGMP-critical process systems, ensuring compliance with regulatory, user and internal requirements.
This role involves hands-on validation work and the preparation and execution of validation documentation within a regulated pharmaceutical environment.
Our client, a prominent pharmaceutical organization, is seeking a Launch Excellence Project Engineer to manage validation aspects for new product introductions. This role ensures successful implementation and regulatory compliance across the product lifecycle, covering formulation, filling, and packaging processes.
Our client, a leading pharmaceutical organization, is looking for a Data Integrity Specialist QA-CSV to support their supply chain systems. This role involves managing quality and compliance for diverse systems within a regulated environment, ensuring data integrity across various operational activities.
Onze klant is een Belgisch bedrijf binnen de farmaceutische sector en kent een indrukwekkend groeiverhaal. Vanuit hun expertise ondersteunen zij andere farmaceutische bedrijven bij de ontwikkeling en productie van geneesmiddelen. Dankzij hun hoogstaande kwaliteit, gespecialiseerde knowhow en klantgerichte aanpak hebben zij een uitstekende reputatie opgebouwd. Vandaag zijn zij uitgegroeid tot een internationaal actieve partner voor tal van toonaangevende spelers binnen de farmaceutische industrie
Onze klant wil in het kader van een naderende pensionering een Technical Services Manager aanwerven.
We zijn op zoek naar een Technical Services Manager die eindverantwoordelijk is voor alle interne technische opvolgingen en daarbij drie teams zal aansturen binnen de domeinen Maintenance, Engineering en Cleaning. Gezien het een farmaceutische omgeving betreft, is ervaring binnen een gereguleerde omgeving een must, bij voorkeur zelfs volgens GMP-standaarden.
In deze functie neem je een belangrijke leiderschapsrol op en stuur je een team van ongeveer 25 à 30 medewerkers aan, waaronder supervisors, techniekers, onderhoudsmedewerkers en engineers.
De locatie van tewerkstelling is in de buurt van Willebroek en Mechelen. Deze functie rapporteert aan de COO.
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Whether you're passionate about regulatory strategy, compliance, or labeling, we offer opportunities across multiple specializations:
Regulatory Strategist – Define and drive regulatory strategy throughout the drug development lifecycle.
Regulatory Affairs Expert – Provide end-to-end regulatory support for development, submission, and post-approval activities.
Regulatory Affairs Specialist – Ensure compliance with EU and global regulations for pharmaceutical products.
Artwork & Labeling Consultant – Manage labeling processes and artwork reviews in line with regulatory guidelines.
Labeling Specialist – Oversee product information and ensure accurate, compliant labeling across markets.
CMC Regulatory Affairs Consultant – Support regulatory submissions related to Chemistry, Manufacturing & Controls (CMC).
Regulatory Project Coordinator – Coordinate timelines, submissions, and stakeholder communication in regulatory projects.
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