Novartis AG
Basel (Land)
QC Analyst II
- 24 June 2026
- 100%
- Basel (Land)
About the job
Summary
~Supports all GxP activities in the Quality department.
Manages quality systems/processes including documentation, metrics and monitoring of actions.
~ Supports the establishment of quality operational processes.
Performs routine GxP compliance/operational activities according to Novartis quality standards. Supports quality projects and initiatives.
Manages quality systems/processes including documentation, metrics and monitoring of actions.
~ Supports the 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
~ Maintains applicable Standard Operating Procedures (SOPs), GxP-compliant documentation and records within the Novartis Quality Management System.
~ Ensures the integrity of all quality assurance records and data, as applicable, and the collaboration of own team with other functions and departments.
~ Ensures an appropriate level of education, GxP knowledge.
~ Updates and manages relevant information in electronic systems (e.g. Change Control, documentation, training).
~ Follows up and monitors e.g. CAPAs, actions, metrics, quality plan.
~ Supports quality audits and inspections by health authorities.
~ Reports technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt.
~ Distribution of promotional samples (if applicable).
Key Performance Indicators
~Supports all GxP activities in the Quality department.
Manages quality systems/processes including documentation, metrics and monitoring of actions.
~ Supports the establishment of quality operational processes.
Performs routine GxP compliance/operational activities according to Novartis quality standards. Supports quality projects and initiatives.
Work Experience
~QC/QA in the pharmaceutical industry/biotechnology with environmental monitoring and cleanroom zones.
~Functional breadth.
~Cross-border collaboration.
Skills
~Technological intelligence.
~QA (Quality Assurance).
~GMP procedures.
~Quality standards.
~Quality control (QC) testing.
~Dealing with ambiguity.
~Self-awareness.
~Continuous learning.
~Technological know-how.
Language
English
~ Maintains applicable Standard Operating Procedures (SOPs), GxP-compliant documentation and records within the Novartis Quality Management System.
~ Ensures the integrity of all quality assurance records and data, as applicable, and the collaboration of own team with other functions and departments.
~ Ensures an appropriate level of education, GxP knowledge.
~ Updates and manages relevant information in electronic systems (e.g. Change Control, documentation, training).
~ Follows up and monitors e.g. CAPAs, actions, metrics, quality plan.
~ Supports quality audits and inspections by health authorities.
~ Reports technical complaints / adverse events / special case scenarios related to Novartis products within 24 hours of receipt.
~ Distribution of promotional samples (if applicable).
Key Performance Indicators
~Supports all GxP activities in the Quality department.
Manages quality systems/processes including documentation, metrics and monitoring of actions.
~ Supports the establishment of quality operational processes.
Performs routine GxP compliance/operational activities according to Novartis quality standards. Supports quality projects and initiatives.
Work Experience
~QC/QA in the pharmaceutical industry/biotechnology with environmental monitoring and cleanroom zones.
~Functional breadth.
~Cross-border collaboration.
Skills
~Technological intelligence.
~QA (Quality Assurance).
~GMP procedures.
~Quality standards.
~Quality control (QC) testing.
~Dealing with ambiguity.
~Self-awareness.
~Continuous learning.
~Technological know-how.
Language
English
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