csv

KYMOS GROUP, a growing CRO with HQ in Spain, seeks a Computer System Validation professional for the Barcelona area. You will support validation of laboratory and other computerized systems in regulated GxP environments, ensuring regulatory compliance and data integrity.You will collaborate with QA, IT and Laboratory teams, handling validation plans, risk...

Qualitice sucht CSV Consultants! Für kommende Projekte im Life-Sciences-Umfeld erweitern wir aktuell unser Team und Netzwerk und suchen Computer System Validation (CSV) Consultants. Besonders interessant sind Profile mit Erfahrung in einem oder mehreren der folgenden Bereiche: • Computer System Validation (CSV) / GAMP 5 • GMP-regulierte Umgebungen •...

**Consultor/a CSV** **Tu nueva empresa** Te incorporarás a una compañía especializada en consultoría Life Sciences que desarrolla proyectos de validación y cumplimiento normativo para compañías farmacéuticas, biotecnológicas y sanitarias a nivel nacional e internacional. Trabajarás en un entorno altamente regulado, participando en proyectos de...

We are looking for a **Quality Assurance & CSV Officer** with experience in the pharmaceutical industry to join our team. If you enjoy taking on new challenges, working in an international environment, and want to grow with us—this might be your next career move! **Main responsibilities:** - Maintain ISO certifications, ensuring compliance with...

Take your career to the next level with **Amaris Consulting** as an **IT Compliance & CSV Specialist – Data Pipelines & Platforms** . Become part of an international team, thrive in a global group with **€800M turnover and 1,000+ clients worldwide** , and an agile environment by planning the kickoff and follow up on projects. Join Amaris Consulting,...

Boehringer Ingelheim España, S.A. busca un profesional para un rol en QA Systems Product orientado a garantizar el cumplimiento GMP de productos y procesos.Se revisan y aprueban documentos y datos maestros, incluyendo APQRs, CSV y CPV, con un enfoque en validaciones y métodos analíticos. El candidato ideal tiene más de 5 años en la industria...

Roche is seeking a Computer System Validation Lead to oversee compliance and validation of digital solutions in CGT. You will ensure software and systems function as intended, aligned with regulatory standards, while collaborating with product managers, RTEs, developers and stakeholders to empower teams to manufacture and deliver high‑quality...

Computerized Systems Validation (CSV) SpecialistBarcelona | Pharmaceutical Industry | HybridAre you passionate about quality, compliance, and digital transformation within highly regulated environments?We are looking for an experienced Computerized Systems Validation (CSV) Specialist to join a leading international pharmaceutical company and play a key role...

Computerized Systems Validation (CSV) Specialist Barcelona | Pharmaceutical Industry | Hybrid Are you passionate about quality, compliance, and digital transformation within highly regulated environments? We are looking for an experienced Computerized Systems Validation (CSV) Specialist to join a leading international pharmaceutical company and play a key...

INSUD PHARMA busca un/a IT COMPLIANCE JUNIOR para incorporarse en nuestras plantas de Azuqueca de Henares. Se valorará experiencia en validación de sistemas informáticos y cumplimiento normativo.El candidato debe tener formación universitaria en Ciencias, Informática o Electrónica Industrial, dominio de español e inglés y capacidad para trabajar en...

In this role you lead CSV and Test Management for Straumann's Global Business Applications, driving validated ERP and enterprise solutions like SAP and Salesforce. You will shape CSV standards, oversee lifecycle documentation, and support global compliance through training and audits. You will collaborate with IT, QA, and business stakeholders during a...

In this role you lead CSV and Test Management for Straumann’s Global Business Applications, driving validated ERP and enterprise solutions like SAP and Salesforce. You will shape CSV standards, oversee lifecycle documentation, and support global compliance through training and audits. You will collaborate with IT, QA, and business stakeholders during a...

Wir sind Qualitice, eine GxP-Beratung mit Sitz in Barcelona. Unsere Kunden sind Pharma-, Biotech- und Medizintechnikunternehmen im deutschsprachigen Raum. Wir liefern das, was in regulierten Systemeinführungen wirklich zählt: belastbare Validierung, Projekte, die den Termin halten, und Dokumentation, die einer Inspektion standhält. Für laufende und...

Roche Holding AG sucht eine erfahrene Lead-Position im Bereich Computer System Validation (CSV) im CGT-Umfeld. Sie überwachen die Validierung digitaler Lösungen, stellen regulatorische Konformität sicher und arbeiten eng mit Produktmanagern, Entwicklern und Stakeholdern zusammen, um hochwertige pharmazeutische Produkte zuverlässig herzustellen. Sie...

KYMOS GROUP, a growing CRO with HQ in Spain, seeks a Computer System Validation professional for the Barcelona area. You will support validation of laboratory and other computerized systems in regulated GxP environments, ensuring regulatory compliance and data integrity. You will collaborate with QA, IT and Laboratory teams, handling validation plans, risk...

En pocas palabrasSi desea conocer los requisitos para este puesto, siga leyendo para obtener toda la información relevante.Posición: Técnico/a Garantía de Calidad en Validaciones y Cualificaciones (CSV/CQV)Localización: Azuqueca de Henares.Experiencia: 3 a 4 años en funciones similares.¿Quieres saber más?INSUD PHARMA opera en toda la cadena de valor...

En pocas palabrasAumente sus posibilidades de conseguir una entrevista leyendo la siguiente descripción general de este puesto antes de presentar su candidatura.Posición: Técnico/a Garantía de Calidad en Validaciones y Cualificaciones (CSV/CQV)Localización: Azuqueca de Henares.Experiencia: 3 a 4 años en funciones similares.¿Quieres saber más?INSUD...

Oxford Global Resources in Barcelona is seeking a Computerized Systems Validation (CSV) Specialist to ensure GxP computerized systems stay compliant, reliable, and inspection-ready throughout their lifecycle. You will lead validation projects, apply risk-based methods per GAMP 5, develop IQ/OQ/PQ docs, support upgrades, audits, and cross-functional...

Qualitice ist eine GxP-Beratung mit Fokus auf Validierung und regulierte Systemeinführungen.¿Le gusta esta oportunidad? Asegúrese de inscribirse rápido, ya que se espera un gran volumen de solicitudes. Desplácese hacia abajo para leer la descripción completa del puesto.Wir suchen Verstärkung für anspruchsvolle Mandate in der DACH-Region, oft in...

Straumann Group seeks a seasoned CSV leader to drive validation and test management for global business applications, including SAP/Salesforce. You will shape CSV standards, oversee lifecycle documentation, and support compliance through audits and training. You will collaborate with IT, QA and business stakeholders during digital transformation and...