Major accountabilities:

• Maintains applicable Standard Operating Procedures (SOPs), Non-GxP and GCLP compliant documentation and records within the Novartis Quality Management System.
• Ensures the integrity of all Quality Systems records and data, as applicable and collaboration of own team with other functions and departments -Ensures an adequate level of education, Non-GxP and GCLP knowledge Updates and maintains relevant information in electronic systems (e.g. Change Control, Documentation, Training)
• Follow up and monitoring of e.g. CAPAs, actions, metrics, Quality plan) -Resolves minor technical issues for clinical programs
• Attend Quality Audits and Health Authority inspections
• Review excising Quality standards

Minimum Requirements:

• Ongoing or recently graduated relevant university degree
• Advanced English written and verbal
• Knowledge of Quality documentation system and pharmaceutical industry related topics

Benefits and rewards: 

Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: 

http://www.novartis.com/careers/benefits-rewards 

Commitment to Diversity & Inclusion:

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

Accessibility and accommodation: 

Novartis is committed to working with and providing reasonable accommodation to all individuals. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the recruitment process, or in any order to receive more detailed information about essential functions of a position, please send an e-mail to inclusion.switzerland@novartis.com and let us know the nature of your request and your contact information. Please include the job requisition number in your message.