Our client, a leading pharmaceutical company, is seeking a Cleaning Validation Engineer to specialize in the development and optimization of cleaning processes for production equipment. The role combines technical expertise with operational support to ensure compliance and business continuity within a regulated manufacturing environment.
Our client, a leading pharmaceutical company, is looking for a Commissioning Lead to drive the execution of an ambitious project. This role involves overseeing the entire commissioning lifecycle, bridging the gap between engineering, contractors, and quality departments to ensure successful delivery of critical installations.
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.
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.
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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