Jan 24, 2022

Job Description

•Ensure laboratory processes are performed in compliance with GxP rules
•Control laboratory related documents
•Perform investigation, evaluation and reporting of events, incidents and deviations
•Control and complete distribution of GxP documents according to procedures
•Ensure that the Risk Assessments related to the Quality Assurance are done
•Contribute to the cost effectiveness and development projects concerning the Quality Assurance Department
•Lead quality agreements process between Novartis facilities/departments
•Represent Quality department in all quality discussions, escalations and globally endorsed projects
•Prepare for the audit/inspection and lead the audit/inspection
•Follow up with the Quality system/GMP audit results of the Health Authorities and Novartis Companies
•Ensure that all issues related to the local and Novartis HSE&BC regulations are handled accordingly

Diversity & Inclusion / EEO

Novartis, olağanüstü, dahil edici bir çalışma ortamı sunmak ve hizmet verdiğimiz hastalar ile toplulukları temsil eden çeşitli ekip temsilcileri oluşturmaya kendini adamıştır.

Minimum Requirements

•University degree in Pharmaceuticals, Chemical Engineering or Chemistry
•Minimum 5 years of experience in a similar position at a multinational pharmaceutical company
•Extensive knowledge of GMP
•Excellent communication skills in English
•Preferably SAP knowledge
•Team working and customer oriented mindset
•Ability to work in a fast-paced changing environment
•Detail-oriented, willing to work in a challenging environment
Novartis Technical Operations
Tam Zamanlı
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Nitrosamine CoE Quality Operations Coordinator

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