CSV Engineer - Wavre, Walloon Region

L'ingénier CSV est responsable de la coordination et de la validation des systèmes informatisés et automatisu"es conformément aux exigences ręglementaires. · ...

To support and coordinate quality and validation activities to ensure the validated status of computer systems within automation and IT/OT projects. · ...

We are seeking a CSV Specialist to join our team in Brabant Wallon, Belgium. As a CSV Specialist, you will play a key role in ensuring compliance and integrity of computerized systems within a leading pharmaceutical environment. · ...

This is a quality support project engineer position responsible for ensuring the validated status of computer systems within automation and IT/OT projects. · ...

As a center of excellence in technology innovation and project management the engineering department of our client in Puurs is working on the future of the site. · The ICS team within Puurs is working actively on the automation and integration of systems and data flows All these ...

We are looking for a CSV Validation Specialist to develop and execute validation strategies for CSV projects. · ...

We are seeking a Senior Automation Engineer to join a leading Life Sciences organization, · a current consultant role in industrial automation projects within regulated environments, · leveraging expertise in Systec tools and contributing to projects while ensuring compliance wit ...

We are seeking a Senior Automation Engineer to join a leading Life Sciences organization. · The role focuses on leveraging expertise in Systec tools and contributing to industrial automation projects within regulated environments. · ...

Akkodis busca perfiles CSV / QA CSV para la industria farmacéutica. Se requiere experiencia en validación y análisis de riesgos. · Máster o licenciatura en ingeniería o ciencias; · Experiencia previa en CSV/QACSV/qa/validation/validation equipamiento preferiblemente sector pharma ...

The Equipment Coordinator/TL coordinates laboratory equipment qualification and maintenance. · Maintain all QC laboratory equipment ensuring proper calibration qualification preventive maintenance according to schedule. · Oversee troubleshoot resolution of equipment related issue ...

We are seeking a Quality Assurance Specialist to lead quality assurance oversight for the implementation of automated systems within clinical laboratories. The ideal candidate will have experience in computerized systems validation (CSV) and equipment qualification. · Lead QA ove ...

Amaris Consulting is an independent technology consulting firm providing guidance and solutions to businesses. · ...

Job summary Lead quality assurance oversight for the implementation of automated and computerized systems within clinical laboratories and central scientific teams. Ensure compliance with global regulatory standards and internal quality systems to support pipeline delivery, audit ...

Lead quality assurance oversight for the implementation of automated and computerized systems within clinical laboratories and central scientific teams. Ensure compliance with global regulatory standards and internal quality systems to support pipeline delivery, audit readiness, ...

The candidate will support the implementation of automated systems within clinical laboratories by providing quality assurance oversight. They will ensure compliance with regulatory standards throughout the system lifecycle. · Ensure business processes, equipment, and automated/a ...

We are looking for a Junior CSV Specialist to support the successful implementation of automated and computerized systems within clinical laboratories. · Bachelor's or Master's degree in Life Sciences, Engineering or related field. · ...

Support the successful implementation of automated and computerized systems within clinical laboratories. · ...

We are seeking a Junior QA Validation Computer Systems for our pharmaceutical and biotechnology clients in the Walloon Region. The successful candidate will be responsible for ensuring the quality of computerized systems and automation projects from design to validation and opera ...

This role is essential for ensuring the quality and compliance of computerized systems within a brand-new biological drug substance manufacturing facility, helping to shape a reliable and efficient validation environment. · Own and manage the end-to-end CSV lifecycle for computer ...

This role is essential for ensuring the quality and compliance of computerized systems within a brand-new biological drug substance manufacturing facility helping to shape a reliable and efficient validation environment · The CSV specialist will own and manage the end-to-end CSV ...