requirements in the different countries and regions Supporting submission and response activities (planning, preparation, review, coordination, submission) Ensuring regulatory comp

Requirements: • Demonstrated excellent communication, presentation and management skills. • Worked in interdisciplinary teams with excellent theoretical and scientific knowledge of

Anforderungen in greifbare Konzepte übersetzen, die Sie verständlich an Ihre KollegInnen weitergeben. Gleichzeitig nutzen Sie Ihr fundiertes Wissen im Bereich GxP-Compliance, Mikro

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 Why Novar

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 Division

requirements and technical constraints. Responsible for detailed design, development, and delivery of system solutions Technical Research and Development Labs. You will engage with

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 Division

Requirements: Education Minimum: Science degree (e.g. Chemistry, Pharmacy, Biochemistry, Molecular Biology, Biotechnology, Biology) or equivalent; advanced degree desired Ideally

Requirements: • University degree in Engineering, Pharmacy, Biochemistry, Biotechnology, Chemistry, Microbiology or equivalent • At least 3 years or more experience in MS&T, QC, QA

Requirements: Degree in science, engineering or equivalent. >5 years of practical experience in chemical / pharmaceutical industry or > 3 years of experience in field of expertise

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 Division

Anforderungen Zusammenarbeit bei internen GxP-Audits und Sicherstellung der Einhaltung interner und externer Audit- und Inspektionspläne Assistenz bei Transferprojekten und Validie

Requirements: • Approx. 5 to 8 years in pharmaceutical industry and/or analytical laboratory in GMP environment (ideally with medical devices) • Knowledge of GMP, Quality Control (

Requirements: Education Minimum: Science degree (e.g. Chemistry, Pharmacy, Biochemistry, Molecular Biology, Biotechnology, Biology) or equivalent; advanced degree desired. Minimum

Requirements: Education Minimum: Science degree (e.g. Chemistry, Pharmacy, Biochemistry, Molecular Biology, Biotechnology, Biology) or equivalent; advanced degree desired. Minimum

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 Division