Quality Control Technician

Summary

The QC Technician performs Quality control analysis on finished Product as well as in incoming materials according to cGMP r and SOPs, performs routine GxP Compliance/ Operational activities according to Novartis Quality Standards and makes analysis on 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 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 Italian, 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.

Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people\-and\-culture

Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally.

Read our handbook (PDF 30 MB)

Division
Operations
Business Unit
Quality
Location
Italy
Site
Ivrea
Company / Legal Entity
IT58 (FCRS \= IT058\) Advanced Accelerator Applications Italy Srl
Functional Area
Quality
Job Type
Full time
Employment Type
Temporary (Fixed Term)
Shift Work
No

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