Csv specialist banen in België

The CSV Specialist role at Nalys involves ensuring compliance and integrity of computerized systems within a leading pharmaceutical environment. · ...

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 ...

Joining Nalys means becoming part of a collaborative, agile and forward-thinking team that values excellence innovation and continuous growth. · ...

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 ...

Catalent seeks a CSV Specialist to ensure compliance and integrity of computerized systems within a leading pharmaceutical environment. · ...

You will help ensure compliance of computerized systems related to our Brussels production site. Execute validation projects for production equipment, laboratory automated instruments, and systems. · Contribute to remediation and data integrity projects ensuring compliance with U ...

Ready to take a quality step forward in your professional journey? Would you like to be part of a company offering numerous development opportunities in a multicultural and international environment? · Then keep reading to learn more about this opportunity based at our production ...

We are looking for a CSV Specialist to join our team in Bruges Metropolitan Area, BE. As a CSV Specialist, you will be responsible for executing end-to-end validation projects for computerized systems and laboratory instruments in compliance with GAMP5 and GMP standards. · ...

A key client of BioTalent based in Belgium are looking to onboard a QA CSV specialists for their growing quality assurance unit. · ...

Akodis busca un QA CSV para implementar y mantener sistemas de calidad en actividades CVV para iniciar una nueva zona productiva. · Mise à jour du master plan des activités CVV et qualification associées avec le QA (équipement) · ...

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

We are looking for a CSV expert who is proactive, motivated & autonomous to join our Compliance team based in Belgium. · Creation of all document in Source CD based on the Source CD procedures and on the validation approach (deliverable list) approved by the IT Compliance Lead · ...

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. · ...

Nous recherchons un(e) Spécialiste Assurance Qualité - Validation des Systèmes Informatisés (CSV) pour assurer la conformité des systèmes informatisés utilisés dans nos opérations pharmaceutiques. · ...

This role involves providing quality partnership and oversight on automated systems implementation for Vx Clinical Laboratories & Assay Portfolio. · Ensure compliance with internal requirements and external standards such as GCLP, GCP, and IS0 9001:2015 · ...

I'm currently partnering with a global industry-leading pharmaceutical company that is expanding its manufacturing operations. · ...

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

This role involves ensuring compliance with cGMP standards through the validation of computerized systems. This position requires hands-on involvement and technical expertise in validation processes. · Develop, implement, and execute validation studies for cGMP-critical computeri ...

This position may be a great fit for you if you are detail-oriented, technically adept, and thrive in a compliance-focused environment. · ...

Dans le cadre du démarrage d'une nouvelle zone de production pour l'un de nos clients du secteur pharmaceutique nous recherchons un(e) QA CSV pour renforcer l'équipe. Vos missions principales sont : · Mettre à jour le Master Plan de Validation et Qualification lié aux activités C ...