Requirements: English
Company: Novartis Farmacutica
Region: Stein , Argovia
About the Role
- Sample storage and management - Analytical testing and documentation of drug products, finished products, complaints, stability, and packaging material samples to GxP standards. Includes stability testing, sample storage, and management.
- Analytical documentation of stability samples to GxP standards. Reporting of technical complaints and adverse events.
Key Performance Indicators:
- Orders are processed correctly and promptly.
- No waiting times due to incorrect or delayed orders.
- Deadline adherence: orders completed on time, timely reporting of missed deadlines, minimizing lead times.
- Maintain constant readiness for inspections; no critical complaints from superiors or inspectors.
- Adhere to GMP, GSU guidelines, and SOPs; avoid critical irregularities.
- Identify and implement cost reduction optimizations.
- Complete training plans.
Qualifications:
- Working experience in a laboratory environment within the pharmaceutical industry.
- Sound technical and scientific knowledge of pharmaceuticals or chemicals.
- Experience in analytics, QC, or equivalent fields.
Why Novartis: Helping people with diseases and their families requires more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting, and inspiring each other to achieve breakthroughs that change patients'' lives. Ready to create a brighter future together? Learn more
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