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QUALIFICATIONS AND JOB DESCRIPTION
•Ensure production processes are performed in compliance with GMP rules
•Control batch records and release batches timely in order not to interrupt shipment program
•Perform investigation, evaluation and reporting of complaints and deviations
•Control and complete distribution of documents according to procedures
•Ensure that the Risk Assessments related to the Quality Assurance are done
•Follow up with the Quality system/GMP audit results of the Health Authorities and Novartis Companies
•Contribute to the cost effectiveness and development projects concerning the Quality Assurance Department
•Ensure that all issue related to the local and Novartis HSE&BC regulations are handled accordingly
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
•Preferably SAP knowledge
•Excellent communication skills in English
•Team working and customer oriented mindset
•Ability to work in a fast-paced changing environment
•Detail-oriented, willing to work in a challenging environment