Quality Control Technician

Novartis Farmacéutica; Zaragoza; Presencial; EUR 25.000 - 35.000; Jornada completa

Descripción de la vacante

Novartis Farmacéutica recherche un Técnico de Control de Calidad pour effectuer des analyses de produits finis et de matières premières selon les normes cGMP. Ce rôle exige une expérience en contrôle de qualité, une formation en chimie ou biologie, ainsi que la capacité à travailler en rotations d'horaires, y compris de nuit. Vous serez responsable du suivi des actes de nettoyage, des vérifications microbiologiques, et de la gestion des non-conformités.

Formación

• Expérience précédente dans des entreprises radiopharmaceutiques souhaitée.
• Fluency in Spanish with good knowledge of English.

Responsabilidades

• Effectuer des analyses de lots selon formation spécifique.
• Conduire des tests de matières premières et de produits finis.
• Participer aux activités de qualification et de validation.

Conocimientos

Contrôle de qualité

Documentation

Analyse microbiologique

Conformité Règles GxP

Gestion des non-conformités

Anglais

Educación

Diplôme en chimie ou biologie

Descripción del empleo

The QC Technician performs quality control analysis on finished products as well as incoming materials according to cGMP and SOPs. The role involves routine GxP compliance and operational activities following Novartis quality standards, including analysis of batches and incoming materials according to cGMP rules and SOPs.

About the Role

In this role, you will be required to work in rotating shifts, including night shifts.

Major accountabilities:

1. Perform analysis of batches following specific training.
2. Perform routine maintenance, cleaning, and periodic microbiological verification of pharmaceutical areas; support external specialized personnel in extraordinary maintenance and qualification activities.
3. Verify incoming and outgoing raw materials and materials.
4. Execute calibration, verification, qualification, and validation activities of QC processes and equipment.
5. Oversee manufacturing for QC sampling activities.
6. Conduct raw material and finished product testing, environmental monitoring, and sterility QC testing, reporting results, and managing non-conformances and deviations as per AAA procedures.
7. Support deviation investigations, OOS/OOT/OOE investigations, CAPA follow-up, implementation, and change control management, including procedure and form revisions.
8. Participate in qualification and validation activities as necessary.
9. Prepare documents, forms, and records such as analytical batch records, following good documentation practices.
10. Support internal and external audits and inspections as required.
11. Education: Chemical or biological degree is desirable.
12. Previous experience in radiopharmaceutical companies is desirable.
13. Fluent in Spanish with good knowledge of English.

Why Novartis?

Our purpose is to reimagine medicine to improve and extend people’s lives. We aim to become the most valued and trusted medicines company in the world, driven by our people. Join us in this mission! Learn more: https://www.novartis.com/about/strategy/people-and-culture

Benefits and Rewards

Read our handbook to learn about how we support your growth: https://www.novartis.com/careers/benefits-rewards

Commitment to Diversity and Inclusion

We are dedicated to building an inclusive, diverse work environment that reflects the communities we serve.

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