Resumen
About the Role
Major accountabilities:
- Sample storage and management .
- Analytical testing/documentation of drug product / finished product / complaints / stability / packaging material samples to GxP standards Stability -Testing/Sample storage and management .
- Analytical documentation of stability samples to GxP standards
Key performance indicators:
- Orders are processed correctly and quickly.
- No waiting times due to wrong or delayed order.
- Deadline adherence rate: orders completed on time, all missed deadlines reported in good time, the shortest possible lead time
- Ensure constant readiness for inspection, no critical complaints from superiors and inspectors
- Consistently follow the GMP and GSU guidelines, as well as the SOPs, no critical irregularities
- Finding and implementing optimization options to reduce costs -
Work Experience:
- Sound technical & scientific knowledge of pharmaceutical/ chemical.
- Working experience in Laboratory environment in pharma
- analytics/QC/ELISA equivalent.
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
Join our Novartis Network: Not the right Novartis role for you? Sign up to our talent community to stay connected and learn about suitable career opportunities as soon as they come up: https://talentnetwork.novartis.com/network
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
Novartis is committed to building an outstanding, inclusive work environment and diverse teams' representative of the patients and communities we serve.
