Job Description Summary
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.
Job Description
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 CAPAs, actions, metrics, Quality plan.
* Resolves minor technical issues for clinical programs.
* Attend Quality Audits and Health Authority inspections.
* Review existing Quality standards.
Minimum Requirements:
* Ongoing or recently graduated relevant university degree.
* Advanced English written and verbal skills.
* 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:
https://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.
Skills Desired:
Agility, Audit Management, Business Partnering, Continued Learning, Health Authorities, Influencing Skills, Knowledge Of CAPA, Quality Management, Risk Management, Root Cause Analysis (RCA), Self-Awareness, SOP (Standard Operating Procedure), Technological Expertise.
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