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:
Skills Desired
Collaboration Communication Skills Data Integrity Dealing With Ambiguity Digital saviness Leadership Operational Excellence Problem Solving Skills Regulatory Requirements knowledge
Required Experience:
Unclear Seniority
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 DescriptionMajor Accountabilities:QC/ QA in pharmaceutical ind./ biotech with environmental monitor...
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:
Skills Desired
Collaboration Communication Skills Data Integrity Dealing With Ambiguity Digital saviness Leadership Operational Excellence Problem Solving Skills Regulatory Requirements knowledge
Required Experience:
Unclear Seniority
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