Novartis
Website:
novartis.com
Job details:
Summary
- Supports all GxP activities in the Quality department.
- Administers Quality Systems/ Processes including documentation, metrics and monitoring of actions.
- Supports establishment of Quality operational processes.
- Performs routine GxP Compliance/ Operational activities according to Novartis Quality Standards. Supports Quality Projects and initiatives.
About The Role
Major Accountabilities:
- QC/ QA in pharmaceutical ind./ biotech with environmental monitoring & cleanliness zones, Functional Breadth, Collaborating across boundaries
- Reporting of technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt
- Distribution of marketing samples (where applicable)
Work Experience
- Quality Assurance
- Quality Control
- Quality Management Systems
- Technological Expertise
- Environmental Monitoring
- Release Management
- Good Manufacturing Practices (cGMP)
- Quality Compliance
- Technological Expertise
- Audit & Inspection Management
- SOP (Standard Operation Procedure) Management
- Documentation Management
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
Benefits and Rewards: Learn about all the ways we’ll help you thrive personally and professionally.
Read our handbook (PDF 30 MB)
Click on Apply to know more.