QA Officer Operations

Job Description Summary

-Manages Quality aspects and projects within area of responsibility.
-Ensures and supports overall GxP conformity and Compliance with the Novartis Quality Management Systems.

 

Job Description

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)

Key Performance Indicators:

• On-time and GMP-compliant release of dosage forms
• No complaints about inspections by authorities in your own area of responsibility without these being noticed & communicated beforehand
• Successfully support continuous improvement projects
• Executes batch release in compliance with registration

Work Experience:

• Quality Assurance
• Quality Control
• Quality Management Systems
• Technological Expertise
• Environmental Monitoring
• Release Management
• Good Manufacturing Practices (cGMP)
• Audit & Inspection Management
• Quality Compliance
• Technological Expertise

Skills:

• Collaboration
• Dealing With Ambiguity
• Operational Excellence
• Regulatory requirements knowledge
• Problem Solving Skills
• Leadership
• Communication skills
• Data Integrity
• Digital saviness

Languages:

• English.

 

Skills Desired

Collaboration, Communication Skills, Data Integrity, Dealing With Ambiguity, Digital saviness, Leadership, Operational Excellence, Problem Solving Skills, Regulatory Requirements knowledge

Global pharmaceutical company focused on innovative medicines in oncology, immunology, and neuroscience. Headquartered in Basel, Switzerland.

novartis.com