Quality Control Technician

Novartis Pharma Schweiz; Zaragoza; Presencial; EUR 30.000 - 45.000; Jornada completa

Descripción de la vacante

A leading pharmaceutical company in Zaragoza, Spain, seeks a Quality Control professional. The role involves performing batch analysis, managing QC processes, and working in a dynamic environment, including rotating shifts. Candidates should have a degree in Chemical or Biological fields, fluency in Spanish, and preferably experience in the radiopharmaceutical sector. Join us to be part of a mission to improve and extend people's lives through innovative medicines.

Formación

• Education: Degree in Chemical or Biological fields is desirable.
• Previous experience in radiopharmaceutical companies is desirable.
• Fluency in Spanish and good knowledge of English is required.

Responsabilidades

• Perform analysis of batches following specific training.
• Maintenance and cleaning of pharmaceutical quality control equipment.
• Verification of incoming and outgoing raw materials.
• Calibration and validation of Quality Control processes.
• Oversight on QC sampling activities.
• Testing of Raw Material and Finished Products.
• Support deviation investigations and quality incident management.
• Prepare documents and follow Good Documentation Practices.
• Support internal and external Audits and Inspections.

Conocimientos

Fluent Spanish

Good knowledge of English

Experience in radiopharmaceutical companies

Educación

Chemical or biological degree

Descripción del empleo

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

Major Accountabilities

• Perform the analysis of batches following specific training;
• Perform routine maintenance and cleaning, periodic microbiological verification of pharmaceutical areas quality control equipment and support external specialized personnel in carrying out extraordinary maintenance/qualification activities;
• Perform incoming and outgoing verification activities of raw materials and materials;
• Execute the calibration, verification, qualification and validation activities of the Quality Control processes and equipment
• Responsible for the oversight on manufacturing for QC sampling activities.
• Raw Material and Finished Product testing, Environmental Monitoring and Sterility QC testing, and reporting of the QC results. Escalation in case of non-conformances and deviations and manage these quality incidents as per AAA procedures.
• Support deviation investigations, OOS/OOT/OOE investigations, CAPA follow up and implementation, and Change Control management, including procedure and form revisions.
• Participation in assigned qualification/validation activities, as necessary.
• Prepares applicable documents, forms, and records such as analytical batch records and follows Good Documentation Practices.
• Support internal and external Audits and Inspections, as required.

Minimum Requirements

• Education: Chemical or biological degree is desirable.
• Previous experience in radiopharmaceutical companies is desirable
• Fluent Spanish, good knowledge of English.

Why Novartis?

Our purpose is to reimagine medicine to improve and extend people’s lives and our vision is to become the most valued and trusted medicines company in the world. How can we achieve this? With our people. It is our associates that drive us each day to reach our ambitions. Be a part of this mission and join us! Learn more here: https://www.novartis.com/about/strategy/people-and-culture

Benefits and rewards

Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards

Commitment To Diversity And Inclusion

Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.