
Quality Assurance Professional for Pharmaceutical Manufacturing
5 days ago
Job Summary
We are seeking a skilled Quality Assurance professional to oversee production and testing activities in our pharmaceutical manufacturing facility.
Key Responsibilities
- Oversight of all production and testing activities to ensure compliance with current Good Manufacturing Practices (cGMP).
- Support exception investigations and review/approve production, quality control, and analytical/Testing records.
- Perform Batch Release in accordance with registration requirements.
- Report technical complaints/adverse events/special case scenarios related to Novartis products within 24 hours.
Essential Requirements
- Timely and compliant release of dosage forms.
- No inspections or complaints from authorities without prior notice and communication.
- Successful support of continuous improvement projects.
Desirable Requirements
- Functional breadth in QC/QA for pharmaceutical industry/biotech with environmental monitoring.
- Collaboration across boundaries.
- Familiarity with cleanliness zones.
Skills
- Continuous learning and adaptability.
- Effective dealing with ambiguity and uncertainty.
- Expertise in GMP procedures, QA, and Quality Control (QC) Testing.
- Awareness of quality standards and ability to self-reflect.
- Technological expertise and intelligence.
Languages:
- English.
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