This is a great opportunity to learn from the local quality managers, support them in all allocated tasks like review of quality standard documents and more.
This is a 2 month temporary position from June 1st to July 31st.
About the Role
Major accountabilities:
1. Maintains applicable Standard Operating Procedures (SOPs), Non-GxP and GCLP compliant documentation and records within the Novartis Quality Management System.
2. Ensures the integrity of all Quality Systems records and data, as applicable and collaboration of own team with other functions and departments.
3. Ensures an adequate level of education, Non-GxP and GCLP knowledge.
4. Updates and maintains relevant information in electronic systems (e.g. Change Control, Documentation, Training).
5. Follow up and monitoring of e.g. CAPAs, actions, metrics, Quality plan.
6. Resolves minor technical issues for clinical programs.
7. Attend Quality Audits and Health Authority inspections.
8. Review existing Quality standards.
9. Ongoing or recently graduated relevant university degree.
10. Advanced English written and verbal skills.
11. 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:
We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.
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