Jun 21, 2022

Job Description

•Approval of stability reports and trends
•Follow up deviation and MQI management system and CAPAs related with these deviations
•Follow up CAPAs related with Health Authority inspections, Global and Customer Audits
•Follow up customer complaints system and coordinate the investigations
•Follow up the system for returned products and coordinate all activities
•Oversight of all production and testing activities, ensures compliance with cGxP, incl. data integrity & eCompliance
•Support exception investigations
•Review & approval of production, QC, and AS&T records
•Support OpEx improvement projects Qualified Person

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 Pharmacy, Chemical Engineering or Chemistry
•Minimum 2 years of experience in Quality Assurance department at a pharmaceutical company
•Knowledge of cGMP& cGLP and SAP
•Good command of English is required
•Ability to work in a fast-paced changing environment
•Team working and customer oriented mindset
•Good analytical thinking skills
•Good knowledge of MS Office applications
Novartis Technical Operations
Tam Zamanlı
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Quality Assurance Specialist (Temporary)

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