Summary
About the Role
- Internal/external Training in GMP , Good Aseptic practises and Data integrity .
-Support the preparation, issuance, and archiving of controlled documents (SOPs, work instructions, forms).Ensure documentation is accurate, complete, and compliant with data integrity principles (ALCOA).
-Assist in review of batch manufacturing records issuance and review ( and supporting documents under supervision.
-Events Management training including deviations, CAPAs, and change controls.
-Support the implementation and maintenance of quality management systems in line with internal and regulatory requirements.
-Support the Material/ supplier qualification process.
Why Novartis: Helping people with disease and their families takes more than innovative science. It takes a community of smart, passionate people like you. Collaborating, supporting and inspiring each other. Combining to achieve breakthroughs that change patients’ lives. Ready to create a brighter future together? https://www.novartis.com/about/strategy/people-and-culture
Benefits and Rewards: Read our handbook to learn about all the ways we’ll help you thrive personally and professionally: https://www.novartis.com/careers/benefits-rewards
