Our client, a leading pharmaceutical company, is seeking a CSV Validation Engineer to join their team. This role focuses on the validation of software packages and computerized systems to ensure compliance with global regulatory standards.
Onze klant, een vooraanstaande organisatie in de life sciences, zoekt een professional ter ondersteuning van Computer System Validation (CSV) activiteiten. De rol richt zich op het waarborgen dat geautomatiseerde systemen en interfaces binnen GxP-gereguleerde omgevingen voldoen aan alle regelgevende vereisten en kwaliteitsnormen.
Our client, a leading life sciences organization, is seeking a Project Validation Coordinator to support the delivery of project milestones related to validation. This role involves coordinating project teams, managing validation strategies, and maintaining project schedules within a regulated environment.
Onze klant, een toonaangevende organisatie in de farmaceutische sector, zoekt een gedreven Project Engineer om complexe wettelijke vereisten om te zetten in praktische oplossingen. De focus ligt op het waarborgen van de hoogste kwaliteitsstandaarden binnen diverse productieprocessen en systemen.
Onze klant, een vooraanstaand farmaceutisch bedrijf, is op zoek naar een Project Ingenieur Sterilisatie Validatie. In deze rol is men verantwoordelijk voor het waarborgen van steriliteit en veiligheid door de validatie van diverse sterilisatieprocessen voor innovatieve apparatuur en componenten binnen een aseptische productieomgeving.
Our client, a leading organization in the pharmaceutical sector, is looking for an Expert Lab Systems Support Engineer to manage the operational stability and lifecycle of laboratory IT infrastructure. The role involves overseeing computerized systems within regulated environments to ensure performance, security, and full compliance with industry standards.
Our client is looking for a Utilities Project Engineer to support the utilities and process technology teams. This role involves managing technical projects and equipment improvements from design to handover within a complex industrial environment.
Our client, a leading pharmaceutical organization, is seeking a technical expert to provide project-driven support for robust manufacturing operations. This role focuses on sustaining on-market medical devices and combination products through technical improvements, process changes, and risk management activities. The position acts as a bridge between production and R&D to facilitate product launches and ensure continuous improvement.
Onze klant, een toonaangevende organisatie in de farmaceutische sector, is op zoek naar een gedreven ingenieur om de validatie van afvulinstallaties te begeleiden. De focus ligt op het waarborgen van de kwaliteit en continuïteit van de medicijnproductie door technische installaties van de opstartfase tot de finale oplevering te beheren in een hoogtechnologische omgeving.
Whether you're passionate about process validation, computer system validation, or equipment qualification, we have opportunities across multiple specializations:
Process Validation Specialist – Validate manufacturing processes and ensure consistent product quality.
Cleaning Validation Engineer – Develop and execute cleaning validation protocols and studies.
Commissioning Manager – Lead commissioning activities for pharmaceutical facilities and equipment.
CQV Manager – Manage commissioning, qualification, and validation projects end-to-end.
CSV Consultant – Validate computer systems and ensure data integrity compliance.
Risk Assessment Specialist – Conduct risk assessments for validation and qualification activities.
Compliance Engineer – Ensure validation activities meet GMP and regulatory requirements.
Equipment Validation Specialist – Perform IQ, OQ, and PQ for manufacturing equipment.
Cleanroom Validation Specialist – Qualify and validate cleanroom environments and HVAC systems.
Computer Validation Consultant – Validate computerized systems and software applications.
Validation Coordinator – Coordinate validation projects, documentation, and timelines.
MBR Editor – Create and edit Master Batch Records for manufacturing processes.
MBR Designer – Design comprehensive Master Batch Records and production documentation.
MBR Reviewer – Review and approve Master Batch Records for accuracy and compliance.
Master Batch Specialist – Develop master batch documentation and recipes.
Validation Project Manager – Lead validation projects from planning through execution and closure.
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