Expert Science & Technology

Oct 09, 2021

Job Description

500+ Ongoing clinical trials;160+ Projects in clinical development;80+ Major submissions planned 2020-
2022. Novartis GDD (Global Drug Development) oversees the development of new medicines
discovered by our researchers and partners. It drives breakthrough innovations to improve and extend
the lives of millions.

Your key responsibilities:
Your responsibilities include, but are not limited to:
·Independently plan, organize, perform and document scientific experiments/GMP testing/manufacturing plant activities under minimal supervision; handle several activities at a time.Take over responsibility for and utilize special tools/equipment or specialized facilities as an expert;
schedule and perform maintenance and qualification of instruments/equipment
·Proactively identify conflict situations and contribute to solutions -Work according to appropriate
standards for quality, ethics, health, safety, environment protection, and information security; lead
initiatives to ensure continuous improvement.
·Documentation of raw data, evaluate and interpret results; propose and actively support the design
of next experiments. Review and verify raw data generated by others; approval of tests/experiments
performed by others
·Write protocols, scientific reports or lab procedures based on templates or SOPs under minimal
·For technical development units: Develop new methods or optimize existing methods/processes
(lab or plant); contribute to development and implementation of new technologies.Uses professional
concepts and company's policies and procedures to solve a wide range of difficult problems in
imaginative and practical ways. -Contributes to some cost center goals and objectives –
·Establish innovative solutions for verification and control of critical quality attributes, critical material
attributes or critical process parameter in cooperation with other colleagues. Establish control
procedures and specifications and review test procedures.
·Generate scientific documents to hand over to internal and/or external partners (e.g., MST,
TechOps, authorities, external companies) and support generation of international registration
documents under minimal supervision. If assigned this task, maintenance of infrastructure/equipment and required investments (e.g. system ownership). -Generate lab
procedures or SOP’s, generate protocols and reports
·Lead technical meetings during product development at the local level as well as on the level of
SDC network Report and present scientific/technical results internally and contribute to publications,
presentations and patents.

Diversity & Inclusion / EEO

Novartis is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve.

Minimum Requirements

Novartis is committed to building an outstanding, inclusive work environment and diverse team’s representative of the patients and communities we serve.
Global Drug Development
Research & Development
Full Time

Expert Science & Technology

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