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Vind je volgende functie in Regulatory Affairs binnen Life Sciences en help conforme markttoegang en regulatoire excellentie te garanderen bij de toonaangevende bedrijven in België.
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 farmaceutisch bedrijf, is op zoek naar een Quality Project Associate. In deze rol is men verantwoordelijk voor de kwaliteits- en productregistratieactiviteiten om de introductie van nieuwe producten te ondersteunen.
Our client, a leading organization in the biotech and pharmaceutical industry, is seeking a Clean Piping Engineer to manage specialized utility systems. The role focuses on the design and maintenance of piping infrastructure to ensure the safe transport of clean utilities in compliance with industry standards.
Our client, a leading global pharmaceutical organization, is seeking an experienced QA Specialist to serve as a global Quality Representative. The role focuses on consolidating international serialization systems and defining quality requirements for a new automation integration layer across various manufacturing sites.
Our client, a leading biotechnology company specializing in advanced therapies, is seeking a professional to lead manufacturing investigations. The role focus on driving root cause analysis and ensuring process robustness within a cell and gene therapy environment.
Our client, a leading biotechnology organization, is seeking a professional to support the start-up of a new production facility. The project focuses on technical transfers, sterilization validation, and equipment introduction to expand therapeutic manufacturing capacity. This role ensures that all manufacturing processes are developed and validated according to the highest industry standards.
Our client, a leading player in the MedTech industry, is seeking a Senior Clinical Research Associate to manage clinical study activities across multiple sites. This role focuses on overseeing study site performance, conducting comprehensive monitoring visits, and ensuring high-quality data collection for various medical device projects.
Onze klant, een internationale speler in de farmaceutische sector, is op zoek naar een gedreven CSV Engineer om hun kwaliteit en- validatie team te versterken. Je komt terecht in een dynamische werkomgeving waar je de volledige verantwoordelijkheid draagt voor de validatiestatus van IT-systemen binnen een gereguleerde productieomgeving.
Onze klant, een toonaangevende organisatie in de farmaceutische sector, is op zoek naar een Supplier Quality Specialist om de kwaliteit van aangekochte materialen te waarborgen. De focus ligt op het uitvoeren van onderzoeken en het bewaken van de naleving van kwaliteits- en regulatoire standaarden binnen een gereguleerde productieomgeving.
Our client, a leading organization in the life sciences sector, is seeking a dedicated professional to join their laboratory team. The role involves performing and evaluating complex analytical and microbiological tests within a strictly regulated quality control environment.
Our client, a prominent pharmaceutical organization, is looking for a hands-on Production Engineer to provide first-line technical support. This role ensures the continuity of the production line by troubleshooting process issues and coordinating team activities within a regulated environment.
Our client, a leader in the life sciences industry, is seeking a Project Manager to support their engineering and automation department. This role focuses on overseeing process equipment projects and ensuring the successful delivery of complex technical solutions within a regulated manufacturing environment.
Of je nu gespecialiseerd bent in regulatory strategie, compliance of etikettering: bij ons vind je kansen in uiteenlopende specialisaties.
Regulatory Strategist – Bepaal en begeleid de regulatory strategie doorheen het volledige ontwikkeltraject.
Regulatory Affairs Expert – Bied ondersteuning bij de voorbereiding, indiening en opvolging van regulatoire dossiers.
Regulatory Affairs Specialist – Zorg voor naleving van de Belgische, Europese en internationale regelgeving voor geneesmiddelen.
Artwork & Labeling Consultant – Beheer het labelingproces en voer artworkcontroles uit volgens de geldende richtlijnen.
Labeling Specialist – Waak over correcte en conforme productinformatie voor verschillende markten.
CMC Regulatory Affairs Consultant – Verzorg de indiening van regulatoire CMC-dossiers (Chemistry, Manufacturing & Controls).
Regulatory Projectcoördinator – Coördineer deadlines, dossiers en communicatie met stakeholders.
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