Senior Scientist, Biopharmaceutics-IVIVC

Job Description

2023 will potentially see Sandoz become a standalone organization! Already a global market leader in Generics and Biosimilar medicine, this is an exciting, once-in-a-career opportunity to set our own path forward as an independent, purpose-driven organization, and as the founders of a new Sandoz, this is a time of immense opportunity for us all, both professionally and personally!

Together we will shape the future of Sandoz... are you ready to make a difference?
Major Accountabilities
Expertise in leading Gastroplus, Phoenix WinNonlin and DDD Plus software in performing the in-silico simulations to support the generic formulation development
Expertise in Pharmacokinetic modeling and establishment of PBPK and IVIVC models
Guide and collaborate with associates for the in vitro experimentations such as solubility, IDR and development of bio relevant and discriminatory dissolution methods
Review of data from various in vitro experiments and BE studies
Independently write protocols, reports or lab procedures based on templates.
Work in collaboration with multifunctional project team
Independently perform and document in silico modeling and simulation for various biopharmaceutical activities. Thorough knowledge on the functionality of excipients used in OSDs.
Provide documentation and draw relevant conclusions independently and design next experiments; supervise project related scientific/technical activities. Communicate, address and resolve problems (e.g., deviations and unexpected results from experiments) within own and broader area of responsibility; communicate efficiently across organizational interfaces.

Diversity & Inclusion / EEO

We are committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.

Minimum Requirements

10 + years of Experience
Work in collaboration with multifunctional project team
Independently perform and document in silico modeling and simulation for various biopharmaceutical activities. Thorough knowledge on the functionality of excipients used in OSDs.
Provide documentation and draw relevant conclusions independently and design next experiments; supervise project related scientific/technical activities. Communicate, address and resolve problems (e.g., deviations and unexpected results from experiments) within own and broader area of responsibility; communicate efficiently across organizational interfaces.